rs80358079, BRCA1

N. diseases: 6
Source: CURATED ×
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.
Hereditary Breast and Ovarian Cancer Syndrome
2106 0.827 0.200 17 43057147 intron variant C/T snv 0.700 1.000 12 2000 2015
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
2277 0.827 0.200 17 43057147 intron variant C/T snv 0.700 1.000 1 2012 2012
FANCONI ANEMIA, COMPLEMENTATION GROUP S
28 0.827 0.200 17 43057147 intron variant C/T snv 0.700 0
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1390 0.827 0.200 17 43057147 intron variant C/T snv 0.700 0
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.827 0.200 17 43057147 intron variant C/T snv 0.700 0
PANCREATIC CANCER, SUSCEPTIBILITY TO, 4
22 0.827 0.200 17 43057147 intron variant C/T snv 0.700 0