rs3889514

This is a intron variant variant in the CAND2 gene.

GWAS Catalog Trait Associations (1)

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

serum creatinine amount

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.01
p 1.0e-14
N 494,370
Large GWAS
multi-ancestry
Allele C
OR 0.01
p 1.0e-13
N 394,642
Large GWAS
European

About CAND2

Predicted to enable TBP-class protein binding activity. Predicted to be involved in SCF complex assembly; positive regulation of DNA-templated transcription; and protein ubiquitination. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all CAND2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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