rs8007661

This is a intron variant variant in the TRIP11 gene.

GWAS Catalog Trait Associations (2)

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

body height

Allele T
OR 0.04
p 1.0e-18
N 67,452
Large GWAS
East Asian
Allele T
OR 0.42
p 6.0e-10
N 15,821
Large GWAS
European

BMI-adjusted waist circumference

Allele C
OR 0.02
p 2.0e-8
N 160,475
Meta-analysisLarge GWAS
multi-ancestry

ClinVar annotation

Benign☆☆☆
1 submitter
View on ClinVar →

About TRIP11

This gene was identified based on the interaction of its protein product with thyroid hormone receptor beta. This protein is associated with the Golgi apparatus. The N-terminal region of the protein binds Golgi membranes and the C-terminal region binds the minus ends of microtubules; thus, the protein is thought to play a role in assembly and maintenance of the Golgi ribbon structure around the centrosome. Mutations in this gene cause achondrogenesis type IA.[provided by RefSeq, Mar 2010]

View all TRIP11 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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