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 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.880 1.000 11 2007 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.730 1.000 4 2008 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.720 1.000 3 2012 2018
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.720 1.000 3 2006 2010
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.700 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.700 1.000 1 2016 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.020 0.500 2 2008 2016
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2013 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2012 2012
Gout
CUI: C0018099
Disease: Gout
2354 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2015 2015
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2013 2013
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1 2008 2008
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2012 2012
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2011 2011
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2009 2009
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome
5 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2019 2019
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1 2017 2017