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 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.860 1.000 8 2006 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.050 0.800 5 2007 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.020 2 2013 2014
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.020 1.000 2 2007 2012
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2010 2010
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2013 2013
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2009 2009
Takayasu Arteritis
CUI: C0039263
Disease: Takayasu Arteritis
55 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2016 2016