Gene: RAD51L3-RFFL ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137886232
rs137886232
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. 28724667

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: rs561425038
rs561425038
RAD51D ; RAD51L3-RFFL
C 0.700 GeneticVariation CLINVAR Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. 27978560

2017
dbSNP: rs587781756
rs587781756
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability. 28591191

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: rs786203137
rs786203137
RAD51D ; RAD51L3-RFFL
A 0.700 GeneticVariation CLINVAR Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene. 27913932

2017
dbSNP: rs786203137
rs786203137
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene. 27913932

2017
dbSNP: rs1064793952
rs1064793952
RAD51D ; RAD51L3-RFFL
C 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs1064793952
rs1064793952
RAD51D ; RAD51L3-RFFL
C 0.700 GeneticVariation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs137886232
rs137886232
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728

2016
dbSNP: rs137886232
rs137886232
RAD51D ; RAD51L3-RFFL
A 0.700 CausalMutation CLINVAR Use of 5-Hydroxytryptophan Labeled With Carbon 11 in Social Anxiety Disorder. 26720727

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: rs370228071
rs370228071
RAD51D ; RAD51L3-RFFL
A 0.700 GeneticVariation CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104

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

2016
dbSNP: rs730881935
rs730881935
RAD51D ; RAD51L3-RFFL
C 0.700 GeneticVariation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs730882119
rs730882119
RAD51D ; RAD51L3-RFFL
TG 0.700 CausalMutation CLINVAR Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer. 27433846

2016
dbSNP: rs730882119
rs730882119
RAD51D ; RAD51L3-RFFL
TG 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: rs730882119
rs730882119
RAD51D ; RAD51L3-RFFL
TG 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: rs753862052
rs753862052
RAD51D ; RAD51L3-RFFL
TTA 0.700 GeneticVariation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs876658297
rs876658297
RAD51D ; RAD51L3-RFFL
C 0.700 CausalMutation CLINVAR Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. 26822949

2016