rs397516142, MYH7

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.
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 1.000 0.080 14 23425357 missense variant C/A;G;T snv 8.0E-06; 1.6E-05 0.700 1.000 2 2011 2017
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 1.000 0.080 14 23425357 missense variant C/A;G;T snv 8.0E-06; 1.6E-05 0.700 0
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 1.000 0.080 14 23425357 missense variant C/A;G;T snv 8.0E-06; 1.6E-05 0.700 0