Gene: BRCA1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397508883
rs397508883
BRCA1
TTTA 0.700 CausalMutation CLINVAR

dbSNP: rs1555578398
rs1555578398
BRCA1
TTT 0.700 CausalMutation CLINVAR

dbSNP: rs886040240
rs886040240
BRCA1
TTT 0.700 CausalMutation CLINVAR

dbSNP: rs886038003
rs886038003
BRCA1
TTGCC 0.700 CausalMutation CLINVAR

dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR BRCA1 gene mutations may explain more than 80% of excess number of ovarian cancer cases after breast cancer - a population based study from the Western Sweden Health Care region. 20151938

2010
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. 9150154

1997
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer. 11576847

2001
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. 24504028

2014
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation. 11781691

2001
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques. 15951958

2005
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR Detection of germline BRCA1 mutations in breast cancer patients by quantitative messenger RNA in situ hybridization. 8674039

1996
dbSNP: rs80357856
rs80357856
BRCA1
TTCTCA 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer. 18465347

2008
dbSNP: rs1555596663
rs1555596663
BRCA1
TTC 0.700 CausalMutation CLINVAR

dbSNP: rs80357625
rs80357625
BRCA1
TTC 0.700 CausalMutation CLINVAR

dbSNP: rs1567823254
rs1567823254
BRCA1 ; NBR2
TTA 0.700 CausalMutation CLINVAR A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. 16683254

2006
dbSNP: rs80357595
rs80357595
BRCA1
TTA 0.700 CausalMutation CLINVAR

dbSNP: rs1060502332
rs1060502332
BRCA1
TT 0.700 CausalMutation CLINVAR

dbSNP: rs80357989
rs80357989
BRCA1
TGTAATGA 0.700 CausalMutation CLINVAR

dbSNP: rs886038035
rs886038035
BRCA1
TGG 0.700 CausalMutation CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333

2011
dbSNP: rs1555579748
rs1555579748
BRCA1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1555581824
rs1555581824
BRCA1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1555588756
rs1555588756
BRCA1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1555591706
rs1555591706
BRCA1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs80357650
rs80357650
BRCA1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs80357823
rs80357823
BRCA1
TG 0.700 CausalMutation CLINVAR BRCA mutations in Italian breast/ovarian cancer families. 11938448

2002