rs192588356
This is a coding sequence variant variant.
▶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.
Headache
Tsao YC et al. “Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population.” Cephalalgia : an International Journal of Headache 42(3):229-238 (2022)
Allele T
OR 3.35
p 2.0e-8
N 13,906
Large GWAS
East Asian
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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