Gene: RAD51C ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060502601
rs1060502601
RAD51C
A 0.700 CausalMutation CLINVAR

dbSNP: rs1327086366
rs1327086366
RAD51C
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555597132
rs1555597132
RAD51C
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555602159
rs1555602159
RAD51C
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267606997
rs267606997
RAD51C
A 0.700 GeneticVariation CLINVAR Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer. 26740214

2016
dbSNP: rs267606997
rs267606997
RAD51C
A 0.700 GeneticVariation CLINVAR Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations. 25154786

2015
dbSNP: rs267606997
rs267606997
RAD51C
A 0.700 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 0.700 GeneticVariation CLINVAR Mutation of the RAD51C gene in a Fanconi anemia-like disorder. 20400963

2010
dbSNP: rs757128712
rs757128712
RAD51C ; TEX14
A 0.700 GeneticVariation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010
dbSNP: rs759292615
rs759292615
RAD51C ; LOC105371843
A 0.700 GeneticVariation CLINVAR Insights into DNA recombination from the structure of a RAD51-BRCA2 complex. 12442171

2002
dbSNP: rs759292615
rs759292615
RAD51C ; LOC105371843
A 0.700 GeneticVariation CLINVAR Genetic epidemiology of ovarian cancer and prospects for polygenic risk prediction. 29054568

2017
dbSNP: rs760235677
rs760235677
RAD51C
A 0.700 CausalMutation CLINVAR RAD51C is a susceptibility gene for ovarian cancer. 21616938

2011
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Germline mutations in RAD51C in Jewish high cancer risk families. 23117857

2012
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations. 25154786

2015
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. 22451500

2012
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers. 24993905

2014
dbSNP: rs774586107
rs774586107
RAD51C ; LOC105371843
A 0.700 GeneticVariation CLINVAR Germline RAD51C mutations in ovarian cancer susceptibility. 22725699

2013
dbSNP: rs774586107
rs774586107
RAD51C ; LOC105371843
A 0.700 GeneticVariation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015
dbSNP: rs786203945
rs786203945
RAD51C
A 0.700 CausalMutation CLINVAR

dbSNP: rs876658644
rs876658644
RAD51C
A 0.700 GeneticVariation CLINVAR

dbSNP: rs876659874
rs876659874
RAD51C ; LOC105371843
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555593521
rs1555593521
RAD51C
AGAAT 0.700 CausalMutation CLINVAR

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: rs1466185247
rs1466185247
RAD51C
C 0.700 CausalMutation CLINVAR