rs4690098

GWAS Catalog Trait Associations (10)

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

hepatocyte growth factor activator level

Pietzner M et al. Mapping the proteo-genomic convergence of human diseases. Science (new York, N.y.) 374(6569):eabj1541 (2021)
Allele T
OR 0.56
p 1.0e-282
N 10,708
Large GWAS
European

triglyceride measurement

Allele T
OR 0.05
p 4.0e-44
N 153,950
Large GWAS
East Asian
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.03
p 1.0e-15
N 111,667
Large GWAS
East Asian
Allele T
OR 3.01
p 4.0e-14
N 58,701
Large GWAS
East Asian

platelet count

Allele T
OR
p 1.0e-30
N 721,201
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.02
p 2.0e-29
N 499,097
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele T
OR 0.02
p 2.0e-18
N 408,112
Large GWAS
European

testosterone measurement

Allele T
OR 0.03
p 4.0e-18
N 188,507
Large GWAS
European
Allele T
OR
β 0.000
p 5.0e-9
N 158,000
Major Consortium StudyLarge GWAS
European

non-high density lipoprotein cholesterol measurement

Allele T
OR 0.04
p 2.0e-13
N 146,492
Large GWAS
East Asian

C-reactive protein measurement

Allele T
OR 0.02
p 8.0e-12
N 575,531
Large GWAS
European
Koskeridis F et al. Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Nature Communications 13(1):6939 (2022)
Allele T
OR 0.01
p 2.0e-8
N 575,531
Large GWAS
European

choline measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.02
p 3.0e-11
N 450,015
Large GWAS
multi-ancestry

hematocrit

Allele T
OR 0.01
p 2.0e-9
N 928,679
Large GWAS
multi-ancestry

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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