Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769329153
rs769329153
ZFYVE26
C 0.700 GeneticVariation CLINVAR SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. 19805727

2009
dbSNP: rs769329153
rs769329153
ZFYVE26
C 0.700 GeneticVariation CLINVAR Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. 18394578

2008