rs610604, TNFAIP3

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.
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.860 1.000 10 2009 2015
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
80 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.710 1.000 2 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.700 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.010 1.000 1 2007 2007
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.240 6 137878280 intron variant G/T snv 0.58 0.010 1.000 1 2014 2014