Disease: Muscle Weakness ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757725417
rs757725417
Entrez Id: 10989
Gene Symbol: IMMT
IMMT
CUI: C0151786
Disease:
Muscle Weakness 		0.010 GeneticVariation BEFREE The pathogenic events leading to the progressive muscle weakness in patients with a E706K mutation in the head of the myosin heavy chain (MyHC) IIa were analyzed at the muscle cell and motor protein levels. 17005402 2006