Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766264810
rs766264810
A 0.800 CausalMutation CLINVAR

dbSNP: rs766264810
rs766264810
0.800 GeneticVariation UNIPROT

dbSNP: rs863224945
rs863224945
0.800 GeneticVariation UNIPROT

dbSNP: rs863224945
rs863224945
G 0.800 CausalMutation CLINVAR

dbSNP: rs864321669
rs864321669
0.800 GeneticVariation UNIPROT Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. 26026163

2015

dbSNP: rs864321669
rs864321669
0.800 GeneticVariation UNIPROT ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism. 26297558

2016

dbSNP: rs864321669
rs864321669
G 0.800 CausalMutation CLINVAR

dbSNP: rs864321670
rs864321670
T 0.800 CausalMutation CLINVAR Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. 26026163

2015

dbSNP: rs864321670
rs864321670
0.800 GeneticVariation UNIPROT ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism. 26297558

2016

dbSNP: rs864321670
rs864321670
0.800 GeneticVariation UNIPROT Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia. 26026163

2015

dbSNP: rs864321670
rs864321670
T 0.800 CausalMutation CLINVAR ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism. 26297558

2016