rs1980080

GWAS Catalog Trait Associations (3)

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

disorder of pharynx

Allele T
OR 0.93
p 3.0e-12
N 232,365
Large GWAS
European

upper respiratory tract disorder

Allele T
OR 0.96
p 2.0e-8
N 260,405
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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