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 BRCA1 gene-related hereditary susceptibility to breast and ovarian cancer in Latvia. 24797986

2014
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 Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation. 23274591

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 A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. 21702907

2011
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 The contribution of founder mutations in BRCA1 to breast cancer in Belarus. 20507347

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 Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR The 4154delA mutation carriers in the BRCA1 gene share a common ancestry. 19067236

2009
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism. 18397521

2008
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia. 15951956

2005
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR A high proportion of founder BRCA1 mutations in Polish breast cancer families. 15146557

2004
dbSNP: rs80357711
rs80357711
BRCA1
C 0.700 CausalMutation CLINVAR A protein truncating BRCA1 allele with a low penetrance of breast cancer. 15591272

2004
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