rs758548184, NOD2

N. diseases: 5
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.
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1.000 1 2008 2008
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1 2018 2018
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1.000 1 2018 2018
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1.000 1 2018 2018
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1.000 1 2008 2008