Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. 24504028

2014
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation. 23274591

2013
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR An inherited NBN mutation is associated with poor prognosis prostate cancer. 23149842

2013
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ. 22009639

2012
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia. 22032251

2011
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast cancer in Belarus. 20507347

2010
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania. 20345474

2010
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from Belarus. 20569256

2010
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. UKCCCR Familial Ovarian Cancer Study Group. 8644703

1996