Variant: rs11670056 

    present in Gene: ELL
    present in Chromosome: 19
    Position on Chromosome: 18479133
    Alleles of this Variant: C/T

rs11670056 in ELL gene and Coronary Artery Disease PMID 29212778 2018 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

rs11670056 in ELL gene and Corpuscular Hemoglobin Concentration Mean PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.