rs73159540

This variant is located in the TMEM132D gene.

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GWAS Catalog Trait Associations (1)

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

Pietzner M et al. “Mapping the proteo-genomic convergence of human diseases.” Science (new York, N.y.) 374(6569):eabj1541 (2021)

Allele T

OR 0.32

p 7.0e-60

N 10,708

Large GWAS

European

Sun BB et al. “Genomic atlas of the human plasma proteome.” Nature 558(7708):73-79 (2018)

Allele T

OR —

β 0.270

p 3.0e-12

N 3,301

Large GWAS

European

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Benign

1 submitter

TMEM132D-related disorder

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Gene information from NCBI Gene. Variant classifications from ClinVar.

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