Variant: rs11627485 

    present in Gene: FNTB;CHURC1-FNTB;MAX
    present in Chromosome: 14
    Position on Chromosome: 65020976
    Alleles of this Variant: T/C

rs11627485 in FNTB;CHURC1-FNTB;MAX gene and Corpuscular Hemoglobin Concentration Mean PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs11627485 in FNTB;CHURC1-FNTB;MAX 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.

rs11627485 in FNTB;CHURC1-FNTB;MAX gene and Mean Corpuscular Volume (result) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs11627485 in FNTB;CHURC1-FNTB;MAX gene and Platelet mean volume determination (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs11627485 in FNTB;CHURC1-FNTB;MAX gene and Red Blood Cell Count measurement PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.