rs2968915, ATP6AP2

N. diseases: 3
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.
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 1.000 0.040 X 40580182 intron variant G/A snv 0.010 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 X 40580182 intron variant G/A snv 0.010 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 X 40580182 intron variant G/A snv 0.010 1.000 1 2011 2011