rs117764941

This is a downstream gene variant variant in the PHF20L1 gene.

GWAS Catalog Trait Associations (1)

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

Thyroid stimulating hormone level

Allele A
OR 0.26
p 8.0e-22
N 119,715
Large GWAS
European

About PHF20L1

Enables methylation-dependent protein binding activity. Involved in negative regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleoplasm. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Jul 2025]

View all PHF20L1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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