rs11245981
This is a coding sequence variant variant in the SCGB1C1 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.
uterine fibroid
Kim J et al. “Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups.” Nature Communications 16(1):2273 (2025)
Allele A
OR 0.16
p 7.0e-29
N 709,132
Meta-analysisLarge GWAS
multi-ancestry
About SCGB1C1
Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
View all SCGB1C1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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