rs730880870, MYH7

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.
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.925 0.040 14 23429037 missense variant C/A;T snv 1.2E-05 2.8E-05 0.710 1.000 1 2012 2012
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.040 14 23429037 missense variant C/A;T snv 1.2E-05 2.8E-05 0.010 1.000 1 2012 2012