Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757523840
rs757523840
Entrez Id: 1211;10020
Gene Symbol: CLTA;GNE
CLTA;GNE
CUI: C1853926
Disease:
NONAKA MYOPATHY
C 0.700 CausalMutation CLINVAR Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent. 20059379 2010
dbSNP: rs757523840
rs757523840
Entrez Id: 1211;10020
Gene Symbol: CLTA;GNE
CLTA;GNE
CUI: C1853926
Disease:
NONAKA MYOPATHY
C 0.700 GeneticVariation CLINVAR Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent. 20059379 2010