rs186166891
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
Gormley P et al. “Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.” Nature Genetics 48(8):856-66 (2016)
Allele T
OR 1.09
p 1.0e-15
N 375,752
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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