MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Disease: Obesity ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3782889
rs3782889
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0028754
Disease:
Obesity 		0.010 GeneticVariation BEFREE Effect of obesity on the association between MYL2 (rs3782889) and high-density lipoprotein cholesterol among Korean men. 26763873 2016