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What is the clinical significance of RS1060504824 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1060504824 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1060504824 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1060504824 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1060504824 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1060504824 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1060504824 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1060504824 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1060504824 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1060504824 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1593539513 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/RsRS1593539513 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539513 SNP. | <s>[INST] Which condition is asociated with RS1593539513 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/RsRS1593539513 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539513 SNP. </s> |
In which chromosome is RS1593539513 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593539513 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593539513 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593539513 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593539513 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1593539513 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1593539513 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593539513 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593539513 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593539513 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593539513 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593539513 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593539513 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1593539513 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1555284937 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/RsRS1555284937 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1555284937 SNP. | <s>[INST] Which condition is asociated with RS1555284937 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/RsRS1555284937 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1555284937 SNP. </s> |
In which chromosome is RS1555284937 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1555284937 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1555284937 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1555284937 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1555284937 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1555284937 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1555284937 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1555284937 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1555284937 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1555284937 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1555284937 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1555284937 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1555284937 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1555284937 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1593547275 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/RsRS1593547275 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593547275 SNP. | <s>[INST] Which condition is asociated with RS1593547275 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/RsRS1593547275 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593547275 SNP. </s> |
In which chromosome is RS1593547275 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593547275 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593547275 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593547275 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593547275 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1593547275 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1593547275 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593547275 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593547275 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593547275 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593547275 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593547275 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593547275 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1593547275 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1593446655 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/RsRS1593446655 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593446655 SNP. | <s>[INST] Which condition is asociated with RS1593446655 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/RsRS1593446655 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593446655 SNP. </s> |
In which chromosome is RS1593446655 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593446655 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593446655 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593446655 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593446655 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1593446655 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1593446655 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593446655 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593446655 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593446655 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593446655 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593446655 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593446655 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1593446655 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1593532014 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/RsRS1593532014 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532014 SNP. | <s>[INST] Which condition is asociated with RS1593532014 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/RsRS1593532014 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532014 SNP. </s> |
In which chromosome is RS1593532014 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593532014 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593532014 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593532014 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593532014 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1593532014 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1593532014 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593532014 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593532014 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593532014 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593532014 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593532014 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593532014 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1593532014 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1593434283 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/RsRS1593434283 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593434283 SNP. | <s>[INST] Which condition is asociated with RS1593434283 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/RsRS1593434283 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593434283 SNP. </s> |
In which chromosome is RS1593434283 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593434283 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593434283 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593434283 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593434283 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1593434283 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1593434283 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593434283 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593434283 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593434283 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593434283 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593434283 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593434283 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1593434283 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1060504827 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/RsRS1060504827 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1060504827 SNP. | <s>[INST] Which condition is asociated with RS1060504827 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/RsRS1060504827 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1060504827 SNP. </s> |
In which chromosome is RS1060504827 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1060504827 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1060504827 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1060504827 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1060504827 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1060504827 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1060504827 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1060504827 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1060504827 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1060504827 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1060504827 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1060504827 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1060504827 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1060504827 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS1021965284 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/RsRS1021965284 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1021965284 SNP. | <s>[INST] Which condition is asociated with RS1021965284 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/RsRS1021965284 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1021965284 SNP. </s> |
In which chromosome is RS1021965284 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1021965284 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1021965284 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1021965284 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1021965284 SNP, is it benign or pathogenic? | It is Likely benign. | <s>[INST] What is the clinical significance of RS1021965284 SNP, is it benign or pathogenic? [/INST] It is Likely benign. </s> |
How long is the variation length for RS1021965284 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1021965284 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1021965284 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1021965284 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1021965284 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1021965284 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1021965284 SNP? | The resulting gene consequence is a synonymous variant. | <s>[INST] What is the genetic molecular consequence for RS1021965284 SNP? [/INST] The resulting gene consequence is a synonymous variant. </s> |
Which condition is asociated with RS3092886 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/RsRS3092886 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS3092886 SNP. | <s>[INST] Which condition is asociated with RS3092886 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/RsRS3092886 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS3092886 SNP. </s> |
In which chromosome is RS3092886 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS3092886 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS3092886 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS3092886 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS3092886 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS3092886 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS3092886 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS3092886 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS3092886 SNP? | The origin is germline. | <s>[INST] What is the origin for RS3092886 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS3092886 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS3092886 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS3092886 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS3092886 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS1593455621 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/RsRS1593455621 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593455621 SNP. | <s>[INST] Which condition is asociated with RS1593455621 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/RsRS1593455621 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593455621 SNP. </s> |
In which chromosome is RS1593455621 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593455621 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593455621 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1593455621 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1593455621 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593455621 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593455621 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1593455621 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1593455621 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1593455621 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1593455621 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1593455621 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1593455621 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS1593455621 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |