rs397516089, MYH7

N. diseases: 4
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 0.827 0.080 14 23429807 missense variant C/G;T snv 0.700 1.000 4 2009 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
332 0.827 0.080 14 23429807 missense variant C/G;T snv 0.700 1.000 4 2009 2015
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
19 0.827 0.080 14 23429807 missense variant C/G;T snv 0.700 1.000 3 2009 2015
CARDIOMYOPATHY, DILATED, 1S
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
41 0.827 0.080 14 23429807 missense variant C/G;T snv 0.700 0