rs2277680, CXCL16

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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.020 1.000 2 2010 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.020 1.000 2 2010 2015
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1.000 1 2010 2010
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1.000 1 2010 2010
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1 2011 2011
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1 2008 2008
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1.000 1 2008 2008
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 0.010 1.000 1 2014 2014