Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519181
rs1057519181
0.700 GeneticVariation UNIPROT

dbSNP: rs1064793273
rs1064793273
0.700 GeneticVariation UNIPROT

dbSNP: rs1343258361
rs1343258361
0.700 GeneticVariation UNIPROT

dbSNP: rs141944844
rs141944844
0.700 GeneticVariation UNIPROT

dbSNP: rs202152835
rs202152835
0.700 GeneticVariation UNIPROT

dbSNP: rs121908509
rs121908509
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908510
rs121908510
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908511
rs121908511
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908512
rs121908512
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908513
rs121908513
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908514
rs121908514
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908516
rs121908516
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs121908518
rs121908518
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs1553317025
rs1553317025
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs1553318238
rs1553318238
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs587777757
rs587777757
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs863224923
rs863224923
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs864622162
rs864622162
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs864622179
rs864622179
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs878854990
rs878854990
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs878854991
rs878854991
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs878854992
rs878854992
0.800 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs144594804
rs144594804
0.700 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs1553316816
rs1553316816
0.700 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999

dbSNP: rs372005558
rs372005558
0.700 GeneticVariation UNIPROT Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999