Disease: Handgrip myotonia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs914586984
rs914586984
Entrez Id: 6329;105371858
Gene Symbol: SCN4A;LOC105371858
SCN4A;LOC105371858
CUI: C1868623
Disease:
Handgrip myotonia 		T 0.700 CausalMutation CLINVAR