rs10151051
This is a intron variant variant in the TXNDC16 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Tinnitus
Clifford RE et al. “Genetic architecture distinguishes tinnitus from hearing loss.” Nature Communications 15(1):614 (2024)
Allele A
OR 5.91
p 3.0e-9
N 481,874
Large GWAS
European
About TXNDC16
Located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Jul 2025]
View all TXNDC16 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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