rs619203, 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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.020 1.000 2 2009 2011
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.010 1.000 1 2008 2008
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.010 1.000 1 2008 2008
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.010 1.000 1 2008 2008
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 0.010 1.000 1 2008 2008