Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060502588
rs1060502588
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502601
rs1060502601
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502605
rs1060502605
CCAAT 0.700 CausalMutation CLINVAR

dbSNP: rs1327086366
rs1327086366
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1413872299
rs1413872299
C 0.700 GeneticVariation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015

dbSNP: rs145310733
rs145310733
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1466185247
rs1466185247
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555593450
rs1555593450
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555593457
rs1555593457
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555593521
rs1555593521
AGAAT 0.700 CausalMutation CLINVAR

dbSNP: rs1555593616
rs1555593616
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555593670
rs1555593670
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555594590
rs1555594590
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1555594912
rs1555594912
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555597132
rs1555597132
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555599090
rs1555599090
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555599288
rs1555599288
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555602141
rs1555602141
T 0.700 CausalMutation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015

dbSNP: rs1555602159
rs1555602159
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555602159
rs1555602159
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1567786326
rs1567786326
G 0.700 CausalMutation CLINVAR

dbSNP: rs1567799818
rs1567799818
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567799943
rs1567799943
C 0.700 GeneticVariation CLINVAR

dbSNP: rs200293302
rs200293302
T 0.700 CausalMutation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015

dbSNP: rs200293302
rs200293302
T 0.700 CausalMutation CLINVAR RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families. 25086635

2014