MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Disease: Cardiomyopathy, Hypertrophic, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782965
rs587782965
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial 		T 0.700 GeneticVariation CLINVAR