rs9989177
This variant is located in the DNAAF2;MGAT2 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
blood protein amount
Gudjonsson A et al. “A genome-wide association study of serum proteins reveals shared loci with common diseases.” Nature Communications 13(1):480 (2022)
Allele T
OR 0.18
p 1.0e-20
N 5,360
Large GWAS
European
N-acylethanolamine-hydrolyzing acid amidase measurement
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele C
OR 0.03
p 9.0e-14
N 47,745
Large GWAS
European
▶ClinVar annotation
Benign★★★☆
10 submitters3 publicationsnot specified; Primary ciliary dyskinesia; Congenital disorder of glycosylation; Primary ciliary dyskinesia 10; not provided
View on ClinVar →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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