rs397507954, BRCA2

N. diseases: 3
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.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
2633 0.925 0.200 13 32363225 missense variant A/G snv 4.0E-06 0.700 1.000 13 2008 2019
Hereditary Breast and Ovarian Cancer Syndrome
2106 0.925 0.200 13 32363225 missense variant A/G snv 4.0E-06 0.700 1.000 13 2002 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.925 0.200 13 32363225 missense variant A/G snv 4.0E-06 0.700 1.000 11 2008 2017