MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Disease: Hypertrophic Cardiomyopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516399
rs397516399
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy 		G 0.700 GeneticVariation CLINVAR