Variant: rs159058 

    present in Gene: NOL4L;LOC101929698
    present in Chromosome: 20
    Position on Chromosome: 32520305
    Alleles of this Variant: A/C;T

rs159058 in NOL4L;LOC101929698 gene and Finding of Mean Corpuscular Hemoglobin PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs159058 in NOL4L;LOC101929698 gene and Mean Corpuscular Volume (result) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs159058 in NOL4L;LOC101929698 gene and Red Blood Cell Count measurement PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs159058 in NOL4L;LOC101929698 gene and Reticulocyte count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.