Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41293461
rs41293461
BRCA1
T 0.700 CausalMutation CLINVAR The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population. 24728189

2014
dbSNP: rs41293461
rs41293461
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 germ-line mutations and tumor characteristics in eastern Chinese women with familial breast cancer. 23175448

2013
dbSNP: rs41293461
rs41293461
BRCA1
T 0.700 CausalMutation CLINVAR A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3' third of the gene. 9760198

1998
dbSNP: rs41293461
rs41293461
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing. 9333265

1997