Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1566147422
rs1566147422
MYL2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs751392310
rs751392310
MYL2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR