rs529038, ROS1

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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1.000 1 2008 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1 2009 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1 2009 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1.000 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.120 6 117301070 missense variant C/G;T snv 0.20 0.19 0.010 1.000 1 2009 2009