Gene: BRCA2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11571833
rs11571833
BRCA2
0.010 GeneticVariation BEFREE Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context. 26455428

2015
dbSNP: rs41293475
rs41293475
BRCA2
0.010 GeneticVariation BEFREE Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer. 16168123

2005
dbSNP: rs80358505
rs80358505
BRCA2
0.010 GeneticVariation BEFREE We found two sequence variants, 240G-->A in the 5' untranslated region and 1455C-->T (S388S) in exon 4, in five familial breast cancer cases. 15084242

2004