Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Mutations in context: implications of BRCA testing in diverse populations. 28918466

2018

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. 26848529

2016

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Massively Parallel Functional Analysis of BRCA1 RING Domain Variants. 25823446

2015

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Seventeen years after BRCA1: what is the BRCA mutation status of the breast cancer patients in Africa? - a systematic review. 23519070

2012

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Recurrent BRCA1 and BRCA2 mutations in breast cancer patients of African ancestry. 22739995

2012

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients. 22034289

2012

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR Evidence for an ancient BRCA1 mutation in breast cancer patients of Yoruban ancestry. 18679828

2009

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 17591842

2007

dbSNP: rs80356936
rs80356936
C 0.700 CausalMutation CLINVAR BRCA1 genetic testing in 106 breast and ovarian cancer families from Southern Italy (Sicily): a mutation analyses. 17221156

2007