### Human
stringlengths
17
391
### Assistant
stringlengths
10
790
text
stringlengths
77
866
What is the clinical significance of RS1316896547 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1316896547 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1316896547 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1316896547 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1316896547 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1316896547 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1316896547 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1316896547 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1316896547 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1316896547 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS201020747 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS201020747 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS201020747 SNP.
<s>[INST] Which condition is asociated with RS201020747 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS201020747 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS201020747 SNP. </s>
In which chromosome is RS201020747 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS201020747 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS201020747 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS201020747 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS201020747 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS201020747 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS201020747 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS201020747 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS201020747 SNP?
The origin is germline.
<s>[INST] What is the origin for RS201020747 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS201020747 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS201020747 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS201020747 SNP?
The resulting gene consequence is a intron variant.
<s>[INST] What is the genetic molecular consequence for RS201020747 SNP? [/INST] The resulting gene consequence is a intron variant. </s>
Which condition is asociated with RS1593411999 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593411999 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593411999 SNP.
<s>[INST] Which condition is asociated with RS1593411999 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593411999 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593411999 SNP. </s>
In which chromosome is RS1593411999 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1593411999 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1593411999 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1593411999 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1593411999 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1593411999 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1593411999 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1593411999 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1593411999 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1593411999 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1593411999 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1593411999 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1593411999 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1593411999 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS1010049143 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1010049143 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1010049143 SNP.
<s>[INST] Which condition is asociated with RS1010049143 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1010049143 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1010049143 SNP. </s>
In which chromosome is RS1010049143 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1010049143 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1010049143 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1010049143 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1010049143 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1010049143 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1010049143 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1010049143 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1010049143 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1010049143 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1010049143 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1010049143 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1010049143 SNP?
The resulting gene consequence is a intron variant.
<s>[INST] What is the genetic molecular consequence for RS1010049143 SNP? [/INST] The resulting gene consequence is a intron variant. </s>
Which condition is asociated with RS1593529908 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593529908 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593529908 SNP.
<s>[INST] Which condition is asociated with RS1593529908 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593529908 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593529908 SNP. </s>
In which chromosome is RS1593529908 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1593529908 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1593529908 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1593529908 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1593529908 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1593529908 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1593529908 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1593529908 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1593529908 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1593529908 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1593529908 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1593529908 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1593529908 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1593529908 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS763895695 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS763895695 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS763895695 SNP.
<s>[INST] Which condition is asociated with RS763895695 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS763895695 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS763895695 SNP. </s>
In which chromosome is RS763895695 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS763895695 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS763895695 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS763895695 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS763895695 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS763895695 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS763895695 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS763895695 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS763895695 SNP?
The origin is germline.
<s>[INST] What is the origin for RS763895695 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS763895695 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS763895695 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS763895695 SNP?
The resulting gene consequence is a intron variant.
<s>[INST] What is the genetic molecular consequence for RS763895695 SNP? [/INST] The resulting gene consequence is a intron variant. </s>
Which condition is asociated with RS780654106 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS780654106 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS780654106 SNP.
<s>[INST] Which condition is asociated with RS780654106 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS780654106 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS780654106 SNP. </s>
In which chromosome is RS780654106 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS780654106 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS780654106 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS780654106 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS780654106 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS780654106 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS780654106 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS780654106 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS780654106 SNP?
The origin is germline.
<s>[INST] What is the origin for RS780654106 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS780654106 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS780654106 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS780654106 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS780654106 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS1014225642 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1014225642 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1014225642 SNP.
<s>[INST] Which condition is asociated with RS1014225642 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1014225642 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1014225642 SNP. </s>
In which chromosome is RS1014225642 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1014225642 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1014225642 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1014225642 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1014225642 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1014225642 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1014225642 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1014225642 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1014225642 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1014225642 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1014225642 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1014225642 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1014225642 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1014225642 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS1593414358 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593414358 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593414358 SNP.
<s>[INST] Which condition is asociated with RS1593414358 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593414358 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593414358 SNP. </s>
In which chromosome is RS1593414358 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1593414358 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1593414358 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1593414358 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1593414358 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1593414358 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1593414358 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1593414358 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1593414358 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1593414358 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1593414358 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1593414358 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1593414358 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1593414358 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS771620677 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS771620677 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS771620677 SNP.
<s>[INST] Which condition is asociated with RS771620677 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS771620677 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS771620677 SNP. </s>
In which chromosome is RS771620677 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS771620677 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS771620677 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS771620677 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS771620677 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS771620677 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS771620677 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS771620677 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS771620677 SNP?
The origin is germline.
<s>[INST] What is the origin for RS771620677 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS771620677 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS771620677 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS771620677 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS771620677 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS1593437266 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593437266 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593437266 SNP.
<s>[INST] Which condition is asociated with RS1593437266 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593437266 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593437266 SNP. </s>
In which chromosome is RS1593437266 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1593437266 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1593437266 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1593437266 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1593437266 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1593437266 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1593437266 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1593437266 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1593437266 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1593437266 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1593437266 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1593437266 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1593437266 SNP?
The resulting gene consequence is a intron variant.
<s>[INST] What is the genetic molecular consequence for RS1593437266 SNP? [/INST] The resulting gene consequence is a intron variant. </s>
Which condition is asociated with RS1379479714 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1379479714 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1379479714 SNP.
<s>[INST] Which condition is asociated with RS1379479714 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1379479714 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1379479714 SNP. </s>
In which chromosome is RS1379479714 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS1379479714 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS1379479714 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS1379479714 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS1379479714 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS1379479714 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS1379479714 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS1379479714 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS1379479714 SNP?
The origin is germline.
<s>[INST] What is the origin for RS1379479714 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS1379479714 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS1379479714 SNP? [/INST] The variation is a single nucleotide variant. </s>
What is the genetic molecular consequence for RS1379479714 SNP?
The resulting gene consequence is a synonymous variant.
<s>[INST] What is the genetic molecular consequence for RS1379479714 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s>
Which condition is asociated with RS775381228 SNP?
Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS775381228 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS775381228 SNP.
<s>[INST] Which condition is asociated with RS775381228 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS775381228 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS775381228 SNP. </s>
In which chromosome is RS775381228 SNP located?
It is located in the chromosome 13.
<s>[INST] In which chromosome is RS775381228 SNP located? [/INST] It is located in the chromosome 13. </s>
Which methods support the evidence found for the RS775381228 SNP?
Associated methods are: clinical testing.
<s>[INST] Which methods support the evidence found for the RS775381228 SNP? [/INST] Associated methods are: clinical testing. </s>
What is the clinical significance of RS775381228 SNP, is it benign or pathogenic?
It is Likely benign.
<s>[INST] What is the clinical significance of RS775381228 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s>
How long is the variation length for RS775381228 SNP?
The variation length is 1 base pairs.
<s>[INST] How long is the variation length for RS775381228 SNP? [/INST] The variation length is 1 base pairs. </s>
What is the origin for RS775381228 SNP?
The origin is germline.
<s>[INST] What is the origin for RS775381228 SNP? [/INST] The origin is germline. </s>
What is the type of genetic variation for RS775381228 SNP?
The variation is a single nucleotide variant.
<s>[INST] What is the type of genetic variation for RS775381228 SNP? [/INST] The variation is a single nucleotide variant. </s>