rs952825245
This variant is located in the SLC25A37 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 T
OR 9.95
p 5.0e-12
N 5,885
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
About SLC25A37
SLC25A37 is a solute carrier localized in the mitochondrial inner membrane. It functions as an essential iron importer for the synthesis of mitochondrial heme and iron-sulfur clusters (summary by Chen et al., 2009 [PubMed 19805291]).[supplied by OMIM, Jan 2011]
View all SLC25A37 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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