rs4979462, TNFSF15

N. diseases: 7
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 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.830 1.000 5 2012 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.720 1.000 3 2005 2016
Biliary cirrhosis
CUI: C0023892
Disease: Biliary cirrhosis
36 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.700 1.000 1 2012 2012
Chilblains
CUI: C0008058
Disease: Chilblains
4 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.010 1.000 1 2018 2018
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.010 1.000 1 2016 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.010 1.000 1 2018 2018
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.010 1.000 1 2014 2014