Variant: rs8082605 

    present in Gene: SLFN12L;LOC107985032
    present in Chromosome: 17
    Position on Chromosome: 35537752
    Alleles of this Variant: G/T

rs8082605 in SLFN12L;LOC107985032 gene and Reticulocyte count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.