Disease: Handgrip myotonia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518865
rs1057518865
Entrez Id: 6329
Gene Symbol: SCN4A
SCN4A
CUI: C1868623
Disease:
Handgrip myotonia 		T 0.700 CausalMutation CLINVAR