rs2341459

This is a intron variant variant in the CAMKMT gene.

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GWAS Catalog Trait Associations (1)

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

body height

Lango Allen H et al. “Hundreds of variants clustered in genomic loci and biological pathways affect human height.” Nature 467(7317):832-8 (2010)

Allele T

OR —

β 0.025

p 8.0e-10

N 133,653

Large GWAS

European

About CAMKMT

This gene encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. The protein contains a AdoMet-binding motif and may play a role in calcium-dependent signaling. [provided by RefSeq, Sep 2012]

View all CAMKMT variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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