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In which chromosome is RS1593443514 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1593443514 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1593443514 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1593443514 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1593443514 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1593443514 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1593443514 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1593443514 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1593443514 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS1593443514 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS1593443514 SNP? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for RS1593443514 SNP?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for RS1593443514 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1593443514 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS1285629437 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/RsRS1285629437 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1285629437 SNP. | <s>[INST]Which condition is asociated with RS1285629437 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/RsRS1285629437 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1285629437 SNP.</s> |
In which chromosome is RS1285629437 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1285629437 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1285629437 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1285629437 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1285629437 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS1285629437 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS1285629437 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1285629437 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1285629437 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS1285629437 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS1285629437 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS1285629437 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS1285629437 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS1285629437 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS955333850 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/RsRS955333850 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS955333850 SNP. | <s>[INST]Which condition is asociated with RS955333850 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/RsRS955333850 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS955333850 SNP.</s> |
In which chromosome is RS955333850 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS955333850 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS955333850 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS955333850 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS955333850 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS955333850 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS955333850 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS955333850 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS955333850 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS955333850 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS955333850 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS955333850 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS955333850 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS955333850 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS749894411 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/RsRS749894411 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS749894411 SNP. | <s>[INST]Which condition is asociated with RS749894411 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/RsRS749894411 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS749894411 SNP.</s> |
In which chromosome is RS749894411 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS749894411 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS749894411 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS749894411 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS749894411 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST]What is the clinical significance of RS749894411 SNP, is it benign or pathogenic?[/INST] It is Likely benign.</s> |
How long is the variation length for RS749894411 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS749894411 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS749894411 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS749894411 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS749894411 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS749894411 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS749894411 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS749894411 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS1177544722 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/RsRS1177544722 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1177544722 SNP. | <s>[INST]Which condition is asociated with RS1177544722 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/RsRS1177544722 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1177544722 SNP.</s> |
In which chromosome is RS1177544722 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1177544722 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1177544722 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1177544722 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1177544722 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST]What is the clinical significance of RS1177544722 SNP, is it benign or pathogenic?[/INST] It is Likely benign.</s> |
How long is the variation length for RS1177544722 SNP? | The variation length is 2 base pairs. | <s>[INST]How long is the variation length for RS1177544722 SNP?[/INST] The variation length is 2 base pairs.</s> |
What is the origin for RS1177544722 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS1177544722 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS1177544722 SNP? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for RS1177544722 SNP?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for RS1177544722 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1177544722 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS1370123231 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/RsRS1370123231 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1370123231 SNP. | <s>[INST]Which condition is asociated with RS1370123231 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/RsRS1370123231 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1370123231 SNP.</s> |
In which chromosome is RS1370123231 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1370123231 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1370123231 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1370123231 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1370123231 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of RS1370123231 SNP, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for RS1370123231 SNP? | The variation length is 8 base pairs. | <s>[INST]How long is the variation length for RS1370123231 SNP?[/INST] The variation length is 8 base pairs.</s> |
What is the origin for RS1370123231 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS1370123231 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS1370123231 SNP? | The variation is a Insertion. | <s>[INST]What is the type of genetic variation for RS1370123231 SNP?[/INST] The variation is a Insertion.</s> |
What is the genetic molecular consequence for RS1370123231 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1370123231 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 2 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 2 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 3 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 3 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 14 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 14 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 22 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 22 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 2 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 2 base pairs.</s> |
What is the origin for RS553094345 SNP? | The origin is unknown. | <s>[INST]What is the origin for RS553094345 SNP?[/INST] The origin is unknown.</s> |
What is the type of genetic variation for RS553094345 SNP? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for RS553094345 SNP?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for RS553094345 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS553094345 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP. | <s>[INST]Which condition is asociated with RS553094345 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/RsRS553094345 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS553094345 SNP.</s> |
In which chromosome is RS553094345 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS553094345 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS553094345 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS553094345 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS553094345 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST]What is the clinical significance of RS553094345 SNP, is it benign or pathogenic?[/INST] It is Benign.</s> |
How long is the variation length for RS553094345 SNP? | The variation length is 3 base pairs. | <s>[INST]How long is the variation length for RS553094345 SNP?[/INST] The variation length is 3 base pairs.</s> |