Variant: rs6855981 

    present in Gene: HTT
    present in Chromosome: 4
    Position on Chromosome: 3146549
    Alleles of this Variant: G/A

rs6855981 in HTT gene and Huntington Disease PMID 22387017 2012 Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.

rs6855981 in HTT gene and White Blood Cell Count procedure PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.