rs45516091, MYH7

N. diseases: 2
Source: CLINVAR ×
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
443 14 23431608 missense variant G/A snv 1.2E-05 7.0E-06 0.700 1.000 1 2008 2008
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
172 14 23431608 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0