Variant: rs1085307097 

    present in Gene: SPG11
    present in Chromosome: 15
    Position on Chromosome: 44620234
    Alleles of this Variant: G/-

rs1085307097 in SPG11 gene and Spastic paraplegia 11, autosomal recessive PMID 17322883 2007 Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.