rs1268647997
This variant is located in the RDH13 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 deficiency
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 A
OR 5.07
p 2.0e-12
N 5,885
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
About RDH13
This gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation of retinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria against oxidative stress. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009]
View all RDH13 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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