Variant: rs587777670 

    present in Gene: ELOVL5
    present in Chromosome: 6
    Position on Chromosome: 53270660
    Alleles of this Variant: C/A;T

rs587777670 in ELOVL5 gene and Spinocerebellar ataxia type 38 PMID 25065913 2014 ELOVL5 mutations cause spinocerebellar ataxia 38.