rs7139079

GWAS Catalog Trait Associations (13)

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

cholesterol to total lipids in very large HDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.03
p 7.0e-50
N 450,015
Large GWAS
multi-ancestry

sex hormone-binding globulin measurement

Allele A
OR 0.01
p 5.0e-28
N 188,908
Large GWAS
European
Allele A
OR 0.03
p 1.0e-21
N 196,901
Large GWAS
European

citrate measurement

Allele G
OR 0.05
p 8.0e-28
N 115,068
Large GWAS
European

phospholipids:total lipids ratio

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 2.0e-27
N 450,015
Large GWAS
multi-ancestry

triglycerides in medium HDL measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 1.0e-25
N 450,015
Large GWAS
multi-ancestry

triglycerides in HDL measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 1.0e-22
N 450,015
Large GWAS
multi-ancestry

level of serpin A11 in blood

Allele A
OR 0.03
p 8.0e-19
N 47,745
Large GWAS
European

cholesterol to total lipids in small HDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 2.0e-18
N 450,015
Large GWAS
multi-ancestry

testosterone measurement

Allele G
OR 0.02
p 1.0e-16
N 188,507
Large GWAS
European

total lipids in large VLDL

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.02
p 3.0e-16
N 450,015
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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