rs115651661
This is a intron variant variant in the CNTN3 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.
vitamin D level
Hendi NN et al. “Rare-Variant Genome-Wide Association and Polygenic Score Assessment of Vitamin D Status in a Middle Eastern Population.” International Journal of Molecular Sciences 26(19) (2025)
Allele C
OR 0.56
p 1.0e-8
N 5,885
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
About CNTN3
Predicted to be involved in cell adhesion. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in neuron projection. [provided by Alliance of Genome Resources, Jul 2025]
View all CNTN3 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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