rs10498767

This is a intron variant variant in the RCAN2 gene.

GWAS Catalog Trait Associations (1)

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

body mass index

Allele C
OR 0.01
p 5.0e-16
N 806,834
Meta-analysisLarge GWAS
European
Sidorenko J et al. Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics 56(11):2352-2360 (2024)
Allele C
OR 0.01
p 3.0e-10
N 650,000
Large GWAS
European

About RCAN2

This gene encodes a member of the regulator of calcineurin (RCAN) protein family. These proteins play a role in many physiological processes by binding to the catalytic domain of calcineurin A, inhibiting calcineurin-mediated nuclear translocation of the transcription factor NFATC1. Expression of this gene in skin fibroblasts is upregulated by thyroid hormone, and the encoded protein may also play a role in endothelial cell function and angiogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]

View all RCAN2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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