rs767164213, ZFYVE26

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Spastic Paraplegia
CUI: C0037772
Disease: Spastic Paraplegia
0.700 GeneticVariation CLINVAR SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum. 19805727 2009
Spastic Paraplegia
CUI: C0037772
Disease: Spastic Paraplegia
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
Spastic paraplegia 15, autosomal recessive
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
0.700 GeneticVariation CLINVAR