rs11229030

This is a intergenic variant variant.

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GWAS Catalog Trait Associations (3)

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

pappalysin-1 measurement

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele T
OR 0.06
p 5.0e-31
N 47,745
Large GWAS
European

pappalysin‐1 measurement

Folkersen L et al. “Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.” Nature Metabolism 2(10):1135-1148 (2020)
Allele T
OR —
β 0.091
p 1.0e-20
N 21,758
Large GWAS
European

Crohn's disease

Kenny EE et al. “A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.” Plos Genetics 8(3):e1002559 (2012)
Allele C
OR 1.15
p 8.0e-9
N 2,994
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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