Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782927
rs587782927
DSP
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587782927
rs587782927
DSP
Left ventricular noncompaction cardiomyopathy
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587782927
rs587782927
DSP
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587782927
rs587782927
DSP
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
C 0.700 GeneticVariation CLINVAR