MYL3, myosin light chain 3, 4634

N. diseases: 37; N. variants: 17
Disease: Ventricular septal hypertrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		0.010 GeneticVariation disease BEFREE Furthermore, the MYL3 Arg94His variant was associated with high disease penetrance and substantial interventricular septal hypertrophy. 26443374 2016