rs1343151, IL23R

N. diseases: 10
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.800 1.000 3 2006 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.050 1.000 5 2009 2020
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.020 0.500 2 2015 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2018 2018
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2012 2012
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1 2008 2008
Pediatric Crohn's disease
CUI: C2931133
Disease: Pediatric Crohn's disease
6 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2013 2013
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.010 1.000 1 2010 2010