rs35883013

This variant is located in the TTC38 gene.

GWAS Catalog Trait Associations (1)

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

X-22162 measurement

Allele A
OR 0.71
p 2.0e-23
N 8,249
Large GWAS
European

ClinVar annotation

Likely Benign☆☆☆
1 submitter
View on ClinVar →

About TTC38

Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

View all TTC38 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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