rs200260229, MYH6

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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.040 14 23384530 missense variant C/A;T snv 4.0E-06; 1.9E-04 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 14 23384530 missense variant C/A;T snv 4.0E-06; 1.9E-04 0.010 1.000 1 2018 2018