rs2298566, SNX19

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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 0.010 1.000 1 2007 2007
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 0.010 1.000 1 2007 2007
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 0.010 1.000 1 2007 2007
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 0.010 1.000 1 2007 2007