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<s>[INST]How long is the variation length for RS1555282775 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1555282775 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1555282775 SNP?[/INST] The variation is a single nucleotide variant.</s> |
<s>[INST]What is the genetic molecular consequence for RS1555282775 SNP?[/INST] The resulting gene consequence is a nonsense.</s> |
<s>[INST]Which condition is asociated with RS1555294600 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/RsRS1555294600 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1555294600 SNP.</s> |
<s>[INST]In which chromosome is RS1555294600 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1555294600 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1555294600 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1555294600 SNP?[/INST] The variation length is 2 base pairs.</s> |
<s>[INST]What is the origin for RS1555294600 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1555294600 SNP?[/INST] The variation is a Insertion.</s> |
<s>[INST]What is the genetic molecular consequence for RS1555294600 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with DEL527719?[/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/RsDEL527719. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL527719.</s> |
<s>[INST]In which chromosome is DEL527719 located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the DEL527719?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of DEL527719, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for DEL527719?[/INST] The variation length is 176171 base pairs.</s> |
<s>[INST]What is the origin for DEL527719?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for DEL527719?[/INST] The variation is a Deletion.</s> |
<s>[INST]Which condition is asociated with RS1566234123 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/RsRS1566234123 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566234123 SNP.</s> |
<s>[INST]In which chromosome is RS1566234123 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566234123 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566234123 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566234123 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1566234123 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566234123 SNP?[/INST] The variation is a Duplication.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566234123 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with RS1566199059 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/RsRS1566199059 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566199059 SNP.</s> |
<s>[INST]In which chromosome is RS1566199059 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566199059 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566199059 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566199059 SNP?[/INST] The variation length is 2 base pairs.</s> |
<s>[INST]What is the origin for RS1566199059 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566199059 SNP?[/INST] The variation is a Deletion.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566199059 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with RS1566186087 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/RsRS1566186087 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566186087 SNP.</s> |
<s>[INST]In which chromosome is RS1566186087 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566186087 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566186087 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566186087 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1566186087 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566186087 SNP?[/INST] The variation is a Insertion.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566186087 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with RS1566233076 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/RsRS1566233076 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566233076 SNP.</s> |
<s>[INST]In which chromosome is RS1566233076 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566233076 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566233076 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566233076 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1566233076 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566233076 SNP?[/INST] The variation is a single nucleotide variant.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566233076 SNP?[/INST] The resulting gene consequence is a nonsense.</s> |
<s>[INST]Which condition is asociated with DEL568222?[/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/RsDEL568222. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL568222.</s> |
<s>[INST]In which chromosome is DEL568222 located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the DEL568222?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of DEL568222, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for DEL568222?[/INST] The variation length is 176179 base pairs.</s> |
<s>[INST]What is the origin for DEL568222?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for DEL568222?[/INST] The variation is a Deletion.</s> |
<s>[INST]Which condition is asociated with DEL568225?[/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/RsDEL568225. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL568225.</s> |
<s>[INST]In which chromosome is DEL568225 located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the DEL568225?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of DEL568225, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for DEL568225?[/INST] The variation length is 132 base pairs.</s> |
<s>[INST]What is the origin for DEL568225?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for DEL568225?[/INST] The variation is a Deletion.</s> |
<s>[INST]Which condition is asociated with RS1131690842 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/RsRS1131690842 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690842 SNP.</s> |
<s>[INST]In which chromosome is RS1131690842 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1131690842 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1131690842 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1131690842 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1131690842 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1131690842 SNP?[/INST] The variation is a Deletion.</s> |
<s>[INST]What is the genetic molecular consequence for RS1131690842 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with RS1566174147 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/RsRS1566174147 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566174147 SNP.</s> |
<s>[INST]In which chromosome is RS1566174147 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566174147 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566174147 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566174147 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1566174147 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566174147 SNP?[/INST] The variation is a Duplication.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566174147 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
<s>[INST]Which condition is asociated with RS1566197747 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/RsRS1566197747 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566197747 SNP.</s> |
<s>[INST]In which chromosome is RS1566197747 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1566197747 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1566197747 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1566197747 SNP?[/INST] The variation length is 1 base pairs.</s> |
<s>[INST]What is the origin for RS1566197747 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1566197747 SNP?[/INST] The variation is a single nucleotide variant.</s> |
<s>[INST]What is the genetic molecular consequence for RS1566197747 SNP?[/INST] The resulting gene consequence is a nonsense.</s> |
<s>[INST]Which condition is asociated with RS1593544647 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/RsRS1593544647 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593544647 SNP.</s> |
<s>[INST]In which chromosome is RS1593544647 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1593544647 SNP?[/INST] Associated methods are: clinical testing.</s> |
<s>[INST]What is the clinical significance of RS1593544647 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
<s>[INST]How long is the variation length for RS1593544647 SNP?[/INST] The variation length is 2 base pairs.</s> |
<s>[INST]What is the origin for RS1593544647 SNP?[/INST] The origin is germline.</s> |
<s>[INST]What is the type of genetic variation for RS1593544647 SNP?[/INST] The variation is a Deletion.</s> |
<s>[INST]What is the genetic molecular consequence for RS1593544647 SNP?[/INST] The resulting gene consequence is a splice acceptor variant.</s> |
<s>[INST]Which condition is asociated with RS1593412272 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/RsRS1593412272 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593412272 SNP.</s> |
<s>[INST]In which chromosome is RS1593412272 SNP located?[/INST] It is located in the chromosome 13.</s> |
<s>[INST]Which methods support the evidence found for the RS1593412272 SNP?[/INST] Associated methods are: clinical testing.</s> |