rs1457092, MYO9B

N. diseases: 8
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.
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.040 0.750 4 2007 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.020 1.000 2 2010 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.020 1.000 2 2016 2016
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.010 1.000 1 2010 2010
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.010 1.000 1 2016 2016
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.010 1.000 1 2010 2010
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.010 1.000 1 2007 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.790 0.320 19 17193427 intron variant C/A snv 0.44 0.010 1.000 1 2007 2007