rs7217547
This is a intron variant variant in the FAM222B 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 measurement
Jansen PR et al. “Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.” Nature Genetics 51(3):394-403 (2019)
Allele C
OR 1.05
p 2.0e-8
N 1,331,010
Large GWAS
European
About FAM222B
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all FAM222B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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