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NFKB1 rs11122898: what the research says

rs11122898
Trait
Moderate evidenceGene: NFKB1

This variant was identified as a novel genome-wide significant locus associated with allergy risk in a large-scale meta-analysis.

Common

Our full long-form research profile for rs11122898 — genotype interpretations, evidence review, and FAQ — is being written and will appear on this page soon.
dbSNP ClinVar GWAS Catalog Google Scholar

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Related variants in NFKB1

rs2305160
NFKB1
Pharmacogenomics
Limited

Variant associated with altered response and risk of adverse effects during immunosuppressive therapy.

rs2230750
NFKB1
Trait
Limited

Common non-coding variant frequently investigated in genetic association studies for autoimmune disorders and complex traits.