rs2738752

This is a regulatory region variant variant in the HLX gene.

GWAS Catalog Trait Associations (1)

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

forced expiratory volume, 25-hydroxyvitamin D3 measurement

Allele G
OR
p 3.0e-8
N 211,264
Meta-analysisLarge GWAS
multi-ancestry

About HLX

Enables sequence-specific DNA binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within several processes, including embryonic digestive tract morphogenesis; enteric nervous system development; and regulation of T-helper cell differentiation. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]

View all HLX variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…