Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908627
rs121908627
CLTA ; GNE
CUI: C0026848
Disease: Myopathy
Myopathy 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886044514
rs886044514
CLTA ; GNE
CUI: C0026848
Disease: Myopathy
Myopathy 		A 0.700 CausalMutation CLINVAR