Variant: rs200079802 

    present in Gene: SPG11;EIF3J
    present in Chromosome: 15
    Position on Chromosome: 44563302
    Alleles of this Variant: C/G

rs200079802 in SPG11;EIF3J gene and Spastic paraplegia 11, autosomal recessive PMID 19194956 2009 SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.