Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR Adding In Silico Assessment of Potential Splice Aberration to the Integrated Evaluation of BRCA Gene Unclassified Variants. 26913838

2016
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 CausalMutation CLINVAR Functional classification of BRCA2 DNA variants by splicing assays in a large minigene with 9 exons. 25382762

2015
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR Functional classification of BRCA2 DNA variants by splicing assays in a large minigene with 9 exons. 25382762

2015
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 CausalMutation CLINVAR Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants. 22505045

2012
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants. 22505045

2012
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS). 21990134

2012
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 CausalMutation CLINVAR A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS). 21990134

2012
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR Mutations in BRCA2 and PALB2 in male breast cancer cases from the United States. 20927582

2011
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. 17924331

2007
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 CausalMutation CLINVAR A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. 17924331

2007
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 CausalMutation CLINVAR RNA-based analysis of BRCA1 and BRCA2 gene alterations. 17011978

2006
dbSNP: rs81002893
rs81002893
BRCA2
G 0.700 GeneticVariation CLINVAR RNA-based analysis of BRCA1 and BRCA2 gene alterations. 17011978

2006