Gene: RAD51C ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782170
rs587782170
RAD51C
C 0.700 CausalMutation CLINVAR

dbSNP: rs587782286
rs587782286
RAD51C
C 0.700 CausalMutation CLINVAR

dbSNP: rs587782533
rs587782533
RAD51C
T 0.700 CausalMutation CLINVAR

dbSNP: rs587782699
rs587782699
RAD51C
GAT 0.700 CausalMutation CLINVAR

dbSNP: rs730881931
rs730881931
RAD51C
C 0.700 GeneticVariation CLINVAR

dbSNP: rs730881932
rs730881932
RAD51C ; LOC105371843
T 0.700 GeneticVariation CLINVAR

dbSNP: rs730881940
rs730881940
RAD51C
GA 0.700 CausalMutation CLINVAR

dbSNP: rs748589398
rs748589398
RAD51C
G 0.700 GeneticVariation CLINVAR

dbSNP: rs754367349
rs754367349
RAD51C
G 0.700 CausalMutation CLINVAR

dbSNP: rs786201909
rs786201909
RAD51C
G 0.700 CausalMutation CLINVAR

dbSNP: rs786202563
rs786202563
RAD51C
T 0.700 CausalMutation CLINVAR

dbSNP: rs786203945
rs786203945
RAD51C
A 0.700 CausalMutation CLINVAR

dbSNP: rs876658644
rs876658644
RAD51C
A 0.700 GeneticVariation CLINVAR

dbSNP: rs876658652
rs876658652
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR

dbSNP: rs876659874
rs876659874
RAD51C ; LOC105371843
A 0.700 CausalMutation CLINVAR

dbSNP: rs587782702
rs587782702
RAD51C
T 0.700 GeneticVariation CLINVAR A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families. 21537932

2011
dbSNP: rs387907159
rs387907159
RAD51C
T 0.700 CausalMutation CLINVAR Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients. 21990120

2012
dbSNP: rs267606999
rs267606999
RAD51C
C 0.700 GeneticVariation CLINVAR ATM- and ATR-mediated phosphorylation of XRCC3 regulates DNA double-strand break-induced checkpoint activation and repair. 23438602

2013
dbSNP: rs267606999
rs267606999
RAD51C
C 0.700 GeneticVariation CLINVAR Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair. 24141787

2014
dbSNP: rs267606999
rs267606999
RAD51C
C 0.700 GeneticVariation CLINVAR Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes. 28829762

2017
dbSNP: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing. 27621404

2016
dbSNP: rs1413872299
rs1413872299
RAD51C
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: rs587781287
rs587781287
RAD51C ; LOC105371843
T 0.700 CausalMutation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015
dbSNP: rs587781995
rs587781995
RAD51C ; LOC105371843
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: rs587782528
rs587782528
RAD51C ; TEX14
T 0.700 CausalMutation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015