rs9639976

This variant is located in the TNRC18 gene.

GWAS Catalog Trait Associations (1)

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

ClinVar annotation

Benign☆☆☆
1 submitter
View on ClinVar →

About TNRC18

Predicted to enable chromatin binding activity. Located in cytosol; mitochondrion; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]

View all TNRC18 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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