rs35994878

This is a intron variant variant in the TCF25 gene.

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GWAS Catalog Trait Associations (1)

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

brain attribute

Liu M et al. “Chromosome 10q24.32 Variants Associate With Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study.” Journal of the American Heart Association 12(23):e030935 (2023)

Allele C

OR 0.11

p 3.0e-8

N 4,150

Large GWAS

multi-ancestry

About TCF25

TCF25 is a member of the basic helix-loop-helix (bHLH) family of transcription factors that are important in embryonic development (Steen and Lindholm, 2008 [PubMed 18068114]).[supplied by OMIM, Sep 2008]

View all TCF25 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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