rs10458
This is a 3 prime utr variant variant in the PUDP gene.
▶GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
androstenediol (3beta,17beta) monosulfate (2) 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 G
OR 0.18
p 6.0e-44
N 6,136
Large GWAS
European
pregnenetriol disulfate 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 G
OR 0.10
p 3.0e-16
N 6,136
Large GWAS
European
pregnanediol-3-glucuronide 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 G
OR 0.11
p 5.0e-16
N 6,136
Large GWAS
European
5alpha-pregnan-3beta,20beta-diol 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 G
OR 0.10
p 4.0e-14
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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