rs5979866

This is a upstream gene variant variant in the PUDP gene.

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GWAS Catalog Trait Associations (5)

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

pregnenediol sulfate (C21H34O5S) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele C
OR 0.10
p 5.0e-15
N 6,136
Large GWAS
European

dehydroepiandrosterone sulphate measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele C
OR 0.10
p 2.0e-14
N 6,136
Large GWAS
European

pregnenediol disulfate (C21H34O8S2) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele C
OR —
β 0.090
p 5.0e-13
N 6,136
Large GWAS
European

X-24546 measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele C
OR —
β 0.090
p 1.0e-11
N 6,136
Large GWAS
European

androstenediol (3beta,17beta) monosulfate (1) measurement

Yin X et al. “Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.” Nature Communications 13(1):1644 (2022)
Allele C
OR —
β 0.080
p 5.0e-11
N 6,136
Large GWAS
European

About PUDP

This gene encodes a member of the haloacid dehalogenase-like (HAD) hydrolase superfamily. The encoded protein has no known biological function. This gene has a pseudogene on chromosome 1. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2010]

View all PUDP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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