Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757128712
rs757128712
RAD51C ; TEX14
T 0.700 CausalMutation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015
dbSNP: rs757128712
rs757128712
RAD51C ; TEX14
T 0.700 CausalMutation CLINVAR Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers. 24993905

2014
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: rs757128712
rs757128712
RAD51C ; TEX14
T 0.700 CausalMutation CLINVAR Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. 20400964

2010