Gene: RAD51L3-RFFL ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1403784434
rs1403784434
RAD51D ; RAD51L3-RFFL
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: rs387906843
rs387906843
RAD51D ; RAD51L3-RFFL
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: rs1555567649
rs1555567649
RAD51D ; RAD51L3-RFFL
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: rs370228071
rs370228071
RAD51D ; RAD51L3-RFFL
A 0.700 GeneticVariation CLINVAR Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma. 28646019

2017
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: rs750621215
rs750621215
RAD51D ; RAD51L3-RFFL
A 0.700 GeneticVariation CLINVAR Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. 28724667

2017
dbSNP: rs753862052
rs753862052
RAD51D ; RAD51L3-RFFL
TTA 0.700 CausalMutation CLINVAR Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results. 28008555

2017
dbSNP: rs137886232
rs137886232
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs1555570242
rs1555570242
RAD51D ; RAD51L3-RFFL
T 0.700 GeneticVariation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs370228071
rs370228071
RAD51D ; RAD51L3-RFFL
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: rs387906843
rs387906843
RAD51D ; RAD51L3-RFFL
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
RAD51D ; RAD51L3-RFFL
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: rs561425038
rs561425038
RAD51D ; RAD51L3-RFFL
C 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 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: rs587781756
rs587781756
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs753862052
rs753862052
RAD51D ; RAD51L3-RFFL
TTA 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: rs772306012
rs772306012
RAD51D ; RAD51L3-RFFL
CA 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: rs1057521922
rs1057521922
RAD51D ; RAD51L3-RFFL
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
RAD51D ; RAD51L3-RFFL
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: rs1403784434
rs1403784434
RAD51D ; RAD51L3-RFFL
A 0.700 GeneticVariation CLINVAR Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations. 26046366

2015
dbSNP: rs1555567610
rs1555567610
RAD51D ; RAD51L3-RFFL
GA 0.700 GeneticVariation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015
dbSNP: rs1555567610
rs1555567610
RAD51D ; RAD51L3-RFFL
GA 0.700 GeneticVariation 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: rs1555570242
rs1555570242
RAD51D ; RAD51L3-RFFL
T 0.700 GeneticVariation CLINVAR Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population. 26261251

2015
dbSNP: rs387906843
rs387906843
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Breast cancer in a RAD51D mutation carrier: case report and review of the literature. 25445424

2015