rs582757, TNFAIP3

N. diseases: 8
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 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.800 1.000 3 2012 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.700 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.700 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.020 1.000 2 2009 2015
AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
CUI: C1845052
Disease: AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
4 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.010 1.000 1 2017 2017
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.010 1.000 1 2009 2009