rs16891867

This is a intron variant variant in the C1QTNF7 gene.

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GWAS Catalog Trait Associations (1)

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

conduct disorder

Dick DM et al. “Genome-wide association study of conduct disorder symptomatology.” Molecular Psychiatry 16(8):800-8 (2011)

Allele G

OR 0.15

p 3.0e-9

N 3,963

Large GWAS

multi-ancestry

About C1QTNF7

Predicted to enable identical protein binding activity. Predicted to be located in extracellular space. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Apr 2025]

View all C1QTNF7 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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