rs17234657, None

N. diseases: 3
Source: ALL
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 0.810 1.000 3 2007 2010
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 0.010 1.000 1 2010 2010
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 0.010 1.000 1 2010 2010