rs7980687
This variant is located in the SBNO1 gene.
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
body height
Wood AR et al. “Defining the role of common variation in the genomic and biological architecture of adult human height.” Nature Genetics 46(11):1173-86 (2014)
Allele A
OR 0.04
p 1.0e-26
N 253,288
Large GWAS
European
insomnia
Watanabe K et al. “Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways.” Nature Genetics 54(8):1125-1132 (2022)
Allele A
OR 0.01
p 1.0e-21
N 1,409,137
Meta-analysisLarge GWAS
European
lean body mass
Harris BHL et al. “New role of fat-free mass in cancer risk linked with genetic predisposition.” Scientific Reports 14(1):7270 (2024)
Allele A
OR 0.01
p 9.0e-18
N 337,739
Large GWAS
European
diastolic blood pressure
Hoffmann TJ et al. “Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.” Nature Genetics 49(1):54-64 (2017)
Allele G
OR 0.20
p 2.0e-11
N 321,262
Large GWAS
multi-ancestry
head circumference
Yang XL et al. “Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis.” Frontiers in Genetics 10:947 (2019)
Allele A
OR 0.09
p 1.0e-9
N 182,902
Large GWAS
European
Taal HR et al. “Common variants at 12q15 and 12q24 are associated with infant head circumference.” Nature Genetics 44(5):532-538 (2012)
Allele A
OR 0.07
p 8.0e-9
N 10,768
Large GWAS
European
About SBNO1
Predicted to enable chromatin DNA binding activity and histone binding activity. Predicted to be involved in several processes, including negative regulation of neuroinflammatory response; positive regulation of neural precursor cell proliferation; and regulation of signal transduction. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
View all SBNO1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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