Variant: rs35362007 

    present in Gene: GLRX5;SNHG10
    present in Chromosome: 14
    Position on Chromosome: 95536861
    Alleles of this Variant: G/A

rs35362007 in GLRX5;SNHG10 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.

PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs35362007 in GLRX5;SNHG10 gene and Mean Corpuscular Volume (result) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs35362007 in GLRX5;SNHG10 gene and Red Blood Cell Count measurement PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.