rs35049558, MYL2

N. diseases: 8
Disease: Septal hypertrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Septal hypertrophy
CUI: C0442887
Disease: Septal hypertrophy
0.010 GeneticVariation BEFREE The mutation Arg58Gln showed also moderate septal hypertrophy, but, in contrast, it was associated with an early onset of clinical manifestation and premature sudden cardiac death. 12404107 2002