rs3772190

This variant is located in the MYNN gene.

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GWAS Catalog Trait Associations (2)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

mean corpuscular hemoglobin concentration

Chen MH et al. “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.” Cell 182(5):1198-1213.e14 (2020)

Allele A

OR —

p 7.0e-18

N 630,125

Large GWAS

multi-ancestry

chromosome, telomeric region length

Wen S et al. “Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis.” Nature Genetics 57(3):572-582 (2025)

Allele A

OR —

β 0.073

p 2.0e-16

N 9,598

Major Consortium StudyLarge GWAS

Hispanic or Latin American

About MYNN

This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010]

View all MYNN variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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