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 Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas. 27767231

2017
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 Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitations. 21305653

2011
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 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 Founder mutations in BRCA1 and BRCA2 genes. 17591843

2007
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancer. 16615107

2006
dbSNP: rs80357636
rs80357636
BRCA1
C 0.700 CausalMutation CLINVAR Founder mutations among the Dutch. 15010701

2004
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 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