rs9972882
This variant is located in the STARD3 gene.
▶GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
uromodulin measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele C
OR 0.03
p 5.0e-16
N 47,745
Large GWAS
European
immunoglobulin alpha fc receptor measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele C
OR 0.04
p 9.0e-15
N 47,745
Large GWAS
European
triglyceride measurement
Hebbar P et al. “Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.” Journal of Lipid Research 59(10):1951-1966 (2018)
Allele A
OR 5.99
p 2.0e-9
N 1,353
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
About STARD3
This gene encodes a member of a subfamily of lipid trafficking proteins that are characterized by a C-terminal steroidogenic acute regulatory domain and an N-terminal metastatic lymph node 64 domain. The encoded protein localizes to the membranes of late endosomes and may be involved in exporting cholesterol. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]
View all STARD3 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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