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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> |