rs9612021

This is a regulatory region variant variant in the TTLL12 gene.

GWAS Catalog Trait Associations (1)

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

level of DnaJ homolog subfamily B member 1 in blood

Allele C
OR 0.07
p 8.0e-33
N 47,745
Large GWAS
European

About TTLL12

Enables histone H4K20me3 reader activity and tubulin binding activity. Involved in negative regulation of type I interferon-mediated signaling pathway and regulation of mitotic cell cycle. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]

View all TTLL12 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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