Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer. 28905878

2017
dbSNP: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2. 27616075

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: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic. 26057125

2015
dbSNP: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Germline mutation in the RAD51B gene confers predisposition to breast cancer. 24139550

2013
dbSNP: rs587781410
rs587781410
RAD51C ; LOC105371843
C 0.700 GeneticVariation CLINVAR Germline RAD51C mutations confer susceptibility to ovarian cancer. 22538716

2012