rs574753165
This variant is located in the SCFD2 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.
insomnia
Hammerschlag AR et al. “Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.” Nature Genetics 49(11):1584-1592 (2017)
Allele G
OR 5.85
p 5.0e-9
N 113,006
Large GWAS
European
About SCFD2
Predicted to be involved in intracellular protein transport and vesicle-mediated transport. [provided by Alliance of Genome Resources, Jul 2025]
View all SCFD2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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