Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs558285072
rs558285072
ZFYVE26
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		A 0.700 GeneticVariation CLINVAR Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum. 27544497

2016