rs2413620

This is a intron variant variant in the TNRC6B gene.

GWAS Catalog Trait Associations (1)

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

uterine fibroid

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.10
p 4.0e-27
N 338,926
Large GWAS
multi-ancestry
Allele G
OR 0.10
p 3.0e-24
N 253,542
Meta-analysisLarge GWAS
East Asian, Central Asian, South Asian

About TNRC6B

Enables RNA binding activity. Involved in positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay; positive regulation of nuclear-transcribed mRNA poly(A) tail shortening; and regulatory ncRNA-mediated gene silencing. Acts upstream of with a positive effect on miRNA-mediated gene silencing by inhibition of translation. Predicted to be located in cytosol. Predicted to be active in P-body and nucleoplasm. Implicated in subserous uterine fibroid and uterine fibroid. [provided by Alliance of Genome Resources, Jul 2025]

View all TNRC6B variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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