rs63750741, FBXO11;MSH6

N. diseases: 4
Source: INFERRED ×
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
0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.710 1.000 2 2004 2005
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 7 2004 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 7 2004 2016
Hereditary Nonpolyposis Colorectal Neoplasms
0.827 0.200 2 47799329 missense variant T/C snv 1.2E-05 0.700 1.000 2 2005 2013