Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606997
rs267606997
RAD51C
A 0.800 GeneticVariation CLINVAR Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility. 22167183

2012
dbSNP: rs267606997
rs267606997
RAD51C
A 0.800 GeneticVariation CLINVAR Mutation of the RAD51C gene in a Fanconi anemia-like disorder. 20400963

2010
dbSNP: rs267606997
rs267606997
RAD51C
A 0.800 CausalMutation CLINVAR

dbSNP: rs267606997
rs267606997
RAD51C
0.800 GeneticVariation UNIPROT Mutation of the RAD51C gene in a Fanconi anemia-like disorder. 20400963

2010
dbSNP: rs267606997
rs267606997
RAD51C
0.800 GeneticVariation UNIPROT Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair. 24141787

2014
dbSNP: rs267606997
rs267606997
RAD51C
A 0.800 GeneticVariation CLINVAR Mammalian RAD51 paralogs protect nascent DNA at stalled forks and mediate replication restart. 26354865

2015
dbSNP: rs1060502601
rs1060502601
RAD51C
A 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs1060502601
rs1060502601
RAD51C
A 0.700 CausalMutation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015
dbSNP: rs1060502605
rs1060502605
RAD51C
C 0.700 CausalMutation CLINVAR

dbSNP: rs1327086366
rs1327086366
RAD51C
A 0.700 GeneticVariation CLINVAR Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan. 24800917

2014
dbSNP: rs1327086366
rs1327086366
RAD51C
A 0.700 GeneticVariation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010
dbSNP: rs1327086366
rs1327086366
RAD51C
A 0.700 GeneticVariation CLINVAR Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients. 21990120

2012
dbSNP: rs145310733
rs145310733
RAD51C
G 0.700 GeneticVariation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010
dbSNP: rs145310733
rs145310733
RAD51C
G 0.700 GeneticVariation CLINVAR Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan. 24800917

2014
dbSNP: rs145310733
rs145310733
RAD51C
G 0.700 GeneticVariation CLINVAR Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients. 21990120

2012
dbSNP: rs1555593616
rs1555593616
RAD51C
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555593715
rs1555593715
RAD51C
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555594864
rs1555594864
RAD51C
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555597094
rs1555597094
RAD51C
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555599288
rs1555599288
RAD51C
T 0.700 GeneticVariation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010
dbSNP: rs1555599288
rs1555599288
RAD51C
T 0.700 GeneticVariation CLINVAR Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients. 21990120

2012
dbSNP: rs1555599288
rs1555599288
RAD51C
T 0.700 GeneticVariation CLINVAR Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan. 24800917

2014
dbSNP: rs1555602141
rs1555602141
RAD51C
T 0.700 CausalMutation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015
dbSNP: rs1567785872
rs1567785872
RAD51C
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567786509
rs1567786509
RAD51C
C 0.700 CausalMutation CLINVAR