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 |
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 |
rs1064795045
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs137886232
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited Mutations in Women With Ovarian Carcinoma.
|
26720728 |
2016 |
rs137886232
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in RAD51D confer susceptibility to ovarian cancer.
|
21822267 |
2011 |
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 |
rs1403784434
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.
|
26046366 |
2015 |
rs1555568293
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555568473
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555570285
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1567727934
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs370228071
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma.
|
28646019 |
2017 |
rs370228071
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Loss of function germline mutations in RAD51D in women with ovarian carcinoma.
|
22986143 |
2012 |
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 |
rs370228071
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutation in the RAD51B gene confers predisposition to breast cancer.
|
24139550 |
2013 |
rs370228071
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination.
|
16717288 |
2006 |
rs387906843
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Breast cancer in a RAD51D mutation carrier: case report and review of the literature.
|
25445424 |
2015 |
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 |
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 |
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 |
rs387906843
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in RAD51D confer susceptibility to ovarian cancer.
|
21822267 |
2011 |
rs387906843
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families.
|
22415235 |
2012 |
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 |
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 |
rs561425038
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|