Variant: rs786204767 

    present in Gene: CPT1C
    present in Chromosome: 19
    Position on Chromosome: 49692361
    Alleles of this Variant: C/T

rs786204767 in CPT1C gene and SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT PMID 25751282 2015 Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.