Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057521922
rs1057521922
A 0.700 CausalMutation CLINVAR Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. 25452441

2015

dbSNP: rs1057521922
rs1057521922
A 0.700 CausalMutation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015

dbSNP: rs1064795045
rs1064795045
A 0.700 GeneticVariation CLINVAR

dbSNP: rs137886232
rs137886232
A 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016

dbSNP: rs137886232
rs137886232
A 0.700 CausalMutation CLINVAR Germline mutations in RAD51D confer susceptibility to ovarian cancer. 21822267

2011

dbSNP: rs1403784434
rs1403784434
A 0.700 GeneticVariation CLINVAR Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2. 29020732

2018

dbSNP: rs1403784434
rs1403784434
A 0.700 GeneticVariation CLINVAR Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations. 26046366

2015

dbSNP: rs1555568293
rs1555568293
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555568473
rs1555568473
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555570285
rs1555570285
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567727934
rs1567727934
A 0.700 CausalMutation CLINVAR

dbSNP: rs370228071
rs370228071
A 0.700 GeneticVariation CLINVAR Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma. 28646019

2017

dbSNP: rs370228071
rs370228071
A 0.700 GeneticVariation CLINVAR Loss of function germline mutations in RAD51D in women with ovarian carcinoma. 22986143

2012

dbSNP: rs370228071
rs370228071
A 0.700 GeneticVariation CLINVAR Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer. 26976419

2016

dbSNP: rs370228071
rs370228071
A 0.700 GeneticVariation CLINVAR Germline mutation in the RAD51B gene confers predisposition to breast cancer. 24139550

2013

dbSNP: rs370228071
rs370228071
A 0.700 GeneticVariation CLINVAR Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination. 16717288

2006

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Breast cancer in a RAD51D mutation carrier: case report and review of the literature. 25445424

2015

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing. 27273131

2016

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Surgical Findings and Outcomes in Premenopausal Breast Cancer Patients Undergoing Oophorectomy: A Multicenter Review From the Society of Gynecologic Surgeons Fellows Pelvic Research Network. 28821472

2018

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer. 27153395

2016

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Germline mutations in RAD51D confer susceptibility to ovarian cancer. 21822267

2011

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families. 22415235

2012

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015

dbSNP: rs387906843
rs387906843
A 0.700 CausalMutation CLINVAR Analysis of RAD51D in ovarian cancer patients and families with a history of ovarian or breast cancer. 23372765

2013

dbSNP: rs561425038
rs561425038
A 0.700 GeneticVariation CLINVAR