rs6057599
This is a upstream gene variant variant in the NOL4L 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
Hautakangas H et al. “Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.” Nature Genetics 54(2):152-160 (2022)
Allele T
OR 1.04
p 9.0e-14
N 873,341
Large GWAS
European
About NOL4L
Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
View all NOL4L variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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