Variant: rs2294450 

    present in Gene: CHTF18;GNG13
    present in Chromosome: 16
    Position on Chromosome: 797597
    Alleles of this Variant: T/C

rs2294450 in CHTF18;GNG13 gene and Finding of Mean Corpuscular Hemoglobin PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.