Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Analysis of BRCA1 variants in double-strand break repair by homologous recombination and single-strand annealing. 23161852

2013
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR A high-throughput functional complementation assay for classification of BRCA1 missense variants. 23867111

2013
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Mechanisms of BRCA1 tumor suppression. 22843421

2012
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 RING function is essential for tumor suppression but dispensable for therapy resistance. 22172724

2011
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence of the most frequent BRCA1 mutations in Polish population. 21503673

2011
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Clinical impact of unclassified variants of the BRCA1 and BRCA2 genes. 21965345

2011
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling. 21520273

2011
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Assessment of human Nter and Cter BRCA1 mutations using growth and localization assays in yeast. 21922593

2011
dbSNP: rs28897672
rs28897672
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: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania. 20345474

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Identification of breast tumor mutations in BRCA1 that abolish its function in homologous DNA recombination. 20103620

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Characterization of BRCA1 ring finger variants of uncertain significance. 19543972

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers. 20180014

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The contribution of founder mutations in BRCA1 to breast cancer in Belarus. 20507347

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families. 20683152

2010
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Haplotype of the C61G BRCA1 mutation in Polish and Jewish individuals. 19594371

2009
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR A yeast recombination assay to characterize human BRCA1 missense variants of unknown pathological significance. 18680205

2009
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Genetic analysis of BRCA1 ubiquitin ligase activity and its relationship to breast cancer susceptibility. 16403807

2006
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR The BRCA1 RING and BRCT domains cooperate in targeting BRCA1 to ionizing radiation-induced nuclear foci. 15569676

2005
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area. 16168118

2005
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 : BARD1 induces the formation of conjugated ubiquitin structures, dependent on K6 of ubiquitin, in cells during DNA replication and repair. 14976165

2004
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Binding and recognition in the assembly of an active BRCA1/BARD1 ubiquitin-ligase complex. 12732733

2003
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics. 12601471

2003
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR Contributions of ATM mutations to familial breast and ovarian cancer. 12810666

2003