rs63750119, FBXO11;MSH6

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.
Hereditary Nonpolyposis Colorectal Cancer
1268 0.925 0.160 2 47806282 missense variant G/A;T snv 4.0E-06 0.700 1.000 4 2014 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.925 0.160 2 47806282 missense variant G/A;T snv 4.0E-06 0.700 1.000 4 2007 2015
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
56 0.925 0.160 2 47806282 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2014 2014
Hereditary Nonpolyposis Colorectal Neoplasms
875 0.925 0.160 2 47806282 missense variant G/A;T snv 4.0E-06 0.700 0