rs770637624, RAD51C

N. diseases: 4
Source: CLINVAR ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.882 0.200 17 58709862 stop gained C/T snv 1.6E-05 1.4E-05 0.700 1.000 3 2014 2017
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
CUI: C3150659
Disease: BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3
23 0.882 0.200 17 58709862 stop gained C/T snv 1.6E-05 1.4E-05 0.700 1.000 2 2014 2017
FANCONI ANEMIA, COMPLEMENTATION GROUP O
CUI: C3150653
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP O
63 0.882 0.200 17 58709862 stop gained C/T snv 1.6E-05 1.4E-05 0.700 1.000 2 2014 2017
Hereditary Breast and Ovarian Cancer Syndrome
CUI: C0677776
Disease: Hereditary Breast and Ovarian Cancer Syndrome
2106 0.882 0.200 17 58709862 stop gained C/T snv 1.6E-05 1.4E-05 0.700 0