MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1566147422
rs1566147422
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0878544
Disease:
Cardiomyopathies
C 0.700 GeneticVariation CLINVAR