rs7819412, XKR6

N. diseases: 6
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.827 0.120 8 11187652 intron variant G/A;T snv 0.800 1.000 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.120 8 11187652 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.120 8 11187652 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.120 8 11187652 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.827 0.120 8 11187652 intron variant G/A;T snv 0.010 1.000 1 2019 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.827 0.120 8 11187652 intron variant G/A;T snv 0.010 1.000 1 2010 2010