rs12597502

This is a intron variant variant in the CHD9 gene.

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GWAS Catalog Trait Associations (1)

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

smoking initiation

Saunders GRB et al. “Genetic diversity fuels gene discovery for tobacco and alcohol use.” Nature 612(7941):720-724 (2022)

Allele G

OR 0.01

p 3.0e-14

N 3,382,012

Large GWAS

European, East Asian, Hispanic or Latin American, African unspecified

About CHD9

Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and DNA helicase activity. Predicted to be involved in chromatin organization. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]

View all CHD9 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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