rs1860545, TNFRSF1A

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.
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 2 2013 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 1 2012 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016
Paranoid Schizophrenia
CUI: C0036349
Disease: Paranoid Schizophrenia
23 0.790 0.200 12 6337611 intron variant G/A snv 0.31 0.010 1.000 1 2017 2017