Variant: rs10015979 

    present in Gene: HTT
    present in Chromosome: 4
    Position on Chromosome: 3107715
    Alleles of this Variant: A/G

rs10015979 in HTT gene and Huntington Disease PMID 22387017 2012 Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.