rs4379368
This is a intron variant variant in the SUGCT 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
Anttila V et al. “Genome-wide meta-analysis identifies new susceptibility loci for migraine.” Nature Genetics 45(8):912-917 (2013)
Allele T
OR 1.11
p 1.0e-9
N 118,710
Meta-analysisLarge GWAS
European
About SUGCT
This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]
View all SUGCT variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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