MYL3, myosin light chain 3, 4634

N. diseases: 37; N. variants: 17
Disease: Left ventricular noncompaction cardiomyopathy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs749941468
rs749941468
Entrez Id: 4634
Gene Symbol: MYL3
MYL3
CUI: C4021133
Disease:
Left ventricular noncompaction cardiomyopathy 		0.010 GeneticVariation BEFREE A novel missense substitution in exon 1 of TPM1 (c.109A>G: p.Lys37Glu) was identified in three affected members of a family with isolated LVNC. 20965760 2011