rs138677194
This is a intron variant variant in the TTC38 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
X-22162 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 A
OR 1.30
p 4.0e-76
N 6,136
Large GWAS
European
About TTC38
Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
View all TTC38 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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