rs371855540, MHRT;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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 14 23415095 missense variant C/T snv 2.0E-05 3.5E-05 0.010 1.000 1 2016 2016
Myopathy
CUI: C0026848
Disease: Myopathy
166 14 23415095 missense variant C/T snv 2.0E-05 3.5E-05 0.010 1.000 1 2016 2016