Publication | Open Access

Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits

Genome-wide Association StudyAllelic VariantPhenotypic VariationTranscription-factor-binding SitesGenotype-phenotype AssociationGeneticsHuman PolymorphismPhenotypic VariabilityGenomicsCell BiologyCommon VariantsTranscription FactorsMedicineFunctional GenomicsVariant Interpretation