Variant: rs137852968 

    present in Gene: MIR103A2;PANK2
    present in Chromosome: 20
    Position on Chromosome: 3916955
    Alleles of this Variant: C/A;T

rs137852968 in MIR103A2;PANK2 gene and Hallervorden-Spatz Syndrome PMID 12058097 2002 HARP syndrome is allelic with pantothenate kinase-associated neurodegeneration.