rs4146922

This variant is located in the LOC112268416 gene.

GWAS Catalog Trait Associations (2)

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

Inguinal hernia

Allele T
OR 1.20
p 9.0e-36
N 275,546
Major Consortium StudyLarge GWAS
European

body height

Allele A
OR 0.06
p 1.0e-25
N 36,227
Meta-analysisLarge GWAS
East Asian

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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