Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119476046
rs119476046
T 0.700 CausalMutation CLINVAR

dbSNP: rs864622269
rs864622269
0.010 GeneticVariation BEFREE The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy. 15742100

2005