rs45544633, MHRT;MYH7

N. diseases: 3
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 1.000 0.080 14 23417174 missense variant G/A snv 0.700 1.000 11 2004 2015
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
332 1.000 0.080 14 23417174 missense variant G/A snv 0.700 1.000 8 2004 2013
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
172 1.000 0.080 14 23417174 missense variant G/A snv 0.700 0