rs12424451

This is a intron variant variant in the PARPBP gene.

GWAS Catalog Trait Associations (1)

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

body height

Allele A
OR 0.05
p 1.0e-263
N 928,679
Large GWAS
multi-ancestry

About PARPBP

Predicted to enable DNA binding activity. Involved in negative regulation of double-strand break repair via homologous recombination. Located in chromatin and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

View all PARPBP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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