rs10927732
This is a intron variant variant in the TMEM51 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.
migraine disorder
Choquet H et al. “New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis.” Communications Biology 4(1):864 (2021)
Allele C
OR 1.07
p 4.0e-8
N 554,569
Meta-analysisLarge GWAS
multi-ancestry
About TMEM51
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
View all TMEM51 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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