Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Earlier Age of Breast Cancer Onset in Israeli BRCA Carriers-Is it a Real Phenomenon? 27533489

2016
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations. 24285858

2014
dbSNP: rs80357636
rs80357636
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: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection. 19949876

2010
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Prediction of BRCA1-association in hereditary non-BRCA1/2 breast carcinomas with array-CGH. 18704682

2009
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Founder mutations in BRCA1 and BRCA2 genes. 17591843

2007
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Histopathological features of breast tumours in BRCA1, BRCA2 and mutation-negative breast cancer families. 15642173

2005
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Histopathological characteristics of BRCA1- and BRCA2-associated intraperitoneal cancer: a clinic-based study. 14574155

2003
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families. 11597388

2001
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes. 9361038

1997
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutation analysis in 86 early onset breast/ovarian cancer patients. 9429140

1997
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families. 9150151

1997
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core. 8807330

1996
dbSNP: rs80357636
rs80357636
BRCA1
CT 0.700 CausalMutation CLINVAR