rs114601774

This is a intron variant variant.

GWAS Catalog Trait Associations (2)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

amygdala volume

Mufford MS et al. The Genetic Architecture of Amygdala Nuclei. Biological Psychiatry 95(1):72-84 (2024)
Allele C
OR 2.63
p 6.0e-11
N 36,352
Large GWAS
multi-ancestry
Allele C
OR 0.24
p 2.0e-10
N 35,474
Large GWAS
European

amount of iron in brain

Allele T
OR 0.20
p 2.0e-8
N 39,533
Major Consortium StudyLarge GWAS
European

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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