Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766264810
rs766264810
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1
CUI: C1832669
Disease:
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		A 0.800 CausalMutation CLINVAR
dbSNP: rs766264810
rs766264810
Entrez Id: 5832
Gene Symbol: ALDH18A1
ALDH18A1
CUI: C1832669
Disease:
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		0.800 GeneticVariation UNIPROT