rs78725346
This is a coding sequence variant variant in the HCG22 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
protein measurement
He B et al. “Genome-wide pQTL analysis of protein expression regulatory networks in the human liver.” Bmc Biology 18(1):97 (2020)
Allele A
OR —
β 0.032
p 3.0e-8
N 287
Small GWAS
multi-ancestry
About HCG22
Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
View all HCG22 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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