rs12410394
This is a intergenic variant variant in the CTXND2 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.
cathepsin S measurement
Png G et al. “Mapping the serum proteome to neurological diseases using whole genome sequencing.” Nature Communications 12(1):7042 (2021)
Allele A
OR 0.52
p 2.0e-82
N 2,893
Large GWAS
European
About CTXND2
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all CTXND2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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