rs145310733
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
|
21990120 |
2012 |
rs145310733
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1466185247
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555591851
|
RAD51C;TEX14
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555593450
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555593457
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555593521
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
AGAAT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555593616
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555593616
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555593670
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555593715
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555594590
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
TA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555594864
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555594912
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555597094
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555597132
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555599090
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555599288
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
|
20400964 |
2010 |
rs1555599288
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.
|
21990120 |
2012 |
rs1555599288
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555599288
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.
|
24800917 |
2014 |
rs1555602141
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Hereditary Breast and Ovarian Cancer Syndrome
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555602141
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
FANCONI ANEMIA, COMPLEMENTATION GROUP O
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
rs1555602141
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
rs1555602159
|
Entrez Id: |
5889 |
Gene Symbol: |
RAD51C |
RAD51C
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|