Source: BEFREE ×
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
456 0.716 0.440 1 67228519 intron variant A/G;T snv 0.850 1.000 5 2006 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
238 0.716 0.440 1 67228519 intron variant A/G;T snv 0.830 1.000 3 2009 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.716 0.440 1 67228519 intron variant A/G;T snv 0.820 1.000 2 2010 2017
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.716 0.440 1 67228519 intron variant A/G;T snv 0.060 0.667 6 2008 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 0.716 0.440 1 67228519 intron variant A/G;T snv 0.030 1.000 3 2009 2018
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
50 0.716 0.440 1 67228519 intron variant A/G;T snv 0.020 1.000 2 2012 2014
Diabetes Mellitus, Non-Insulin-Dependent
1598 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2014 2014
Graves Disease
CUI: C0018213
Disease: Graves Disease
252 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2008 2008
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
39 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2010 2010
Iron deficiency
CUI: C0240066
Disease: Iron deficiency
13 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2017 2017
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
18 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2009 2009
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome
5 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2019 2019
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2008 2008