rs182482858

This is a intron variant variant in the TMEM131 gene.

GWAS Catalog Trait Associations (1)

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

hypothyroidism

Allele C
OR 0.23
p 2.0e-19
N 1,786,062
Large GWAS
European
Figuerêdo J et al. Uncovering the shared genetic components of thyroid disorders and reproductive health. European Journal of Endocrinology 191(2):211-222 (2024)
Allele C
OR 1.28
p 1.0e-10
N 691,986
Large GWAS
European

About TMEM131

Enables collagen binding activity. Involved in collagen biosynthetic process. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all TMEM131 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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