rs750272074, ROS1

N. diseases: 2
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 1.000 0.120 6 117362705 synonymous variant A/G snv 4.0E-06 0.010 1.000 1 2008 2008
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.120 6 117362705 synonymous variant A/G snv 4.0E-06 0.010 1.000 1 2008 2008