rs397516165, MYH7

N. diseases: 4
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.
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 1.000 5 2011 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 1.000 5 2011 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 0
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
47 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 0