Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer. 28423363

2017
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Frequency of germline DNA genetic findings in an unselected prospective cohort of triple-negative breast cancer patients participating in a platinum-based neoadjuvant chemotherapy trial. 27083178

2016
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic. 26057125

2015
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Breast cancer in a RAD51D mutation carrier: case report and review of the literature. 25445424

2015
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants. 24130102

2014
dbSNP: rs587780104
rs587780104
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Loss of function germline mutations in RAD51D in women with ovarian carcinoma. 22986143

2012