rs11135349

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.

major depressive disorder

Allele C
OR 1.03
p 2.0e-30
N 807,553
Meta-analysisLarge GWAS
European
Allele C
OR 0.02
p 2.0e-15
N 1,820,689
Large GWAS
multi-ancestry
Allele C
OR 0.03
p 2.0e-10
N 500,199
Large GWAS
European
Allele C
OR 1.03
p 1.0e-9
N 480,359
Large 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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