rs3790567, IL12RB2

N. diseases: 4
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.800 1.000 2 2009 2010
Biliary cirrhosis
CUI: C0023892
Disease: Biliary cirrhosis
36 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.700 1.000 2 2009 2010
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.010 1.000 1 2011 2011
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.010 1.000 1 2015 2015