rs755492182, ACTN2

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.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.882 0.080 1 236735677 missense variant C/T snv 0.010 1.000 1 2019 2019
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.080 1 236735677 missense variant C/T snv 0.010 1.000 1 2019 2019
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.882 0.080 1 236735677 missense variant C/T snv 0.010 1.000 1 2019 2019