Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018

dbSNP: rs80359187
rs80359187
T 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018

dbSNP: rs80359187
rs80359187
T 0.700 GeneticVariation CLINVAR BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population? 29161300

2017

dbSNP: rs80359187
rs80359187
T 0.700 GeneticVariation CLINVAR Functional assays for analysis of variants of uncertain significance in BRCA2. 24323938

2014

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity. 23108138

2013

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma. 19064968

2009

dbSNP: rs80359187
rs80359187
T 0.700 GeneticVariation CLINVAR Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios. 19043619

2008

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios. 19043619

2008

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR BRCA2 germline mutations in familial pancreatic carcinoma. 12569143

2003

dbSNP: rs80359187
rs80359187
T 0.700 GeneticVariation CLINVAR BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. 12228710

2002

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. 12228710

2002

dbSNP: rs80359187
rs80359187
A 0.700 GeneticVariation CLINVAR Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families. 11149425

2001