rs779640835, RYR2

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.
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 1.000 0.040 1 237566723 missense variant C/A;T snv 4.0E-06; 2.8E-05 0.010 1.000 1 2019 2019
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 1.000 0.040 1 237566723 missense variant C/A;T snv 4.0E-06; 2.8E-05 0.010 1.000 1 2019 2019