rs9925481, CLEC16A

N. diseases: 5
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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 16 11003622 intron variant C/G;T snv 0.730 1.000 4 2009 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.882 0.160 16 11003622 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.160 16 11003622 intron variant C/G;T snv 0.010 1.000 1 2009 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.882 0.160 16 11003622 intron variant C/G;T snv 0.010 1.000 1 2010 2010
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.160 16 11003622 intron variant C/G;T snv 0.010 1.000 1 2010 2010