rs12599637

This is a intergenic variant variant.

GWAS Catalog Trait Associations (8)

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

body mass index

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 9.0e-23
N 523,818
Large GWAS
multi-ancestry

triglyceride measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 1.0e-16
N 455,659
Large GWAS
multi-ancestry

total lipids in medium VLDL

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.02
p 1.0e-14
N 450,015
Large GWAS
multi-ancestry

C-reactive protein measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.02
p 2.0e-14
N 436,491
Large GWAS
multi-ancestry

metabolic syndrome

Lind L et al. Genome-Wide Association Study of the Metabolic Syndrome in UK Biobank. Metabolic Syndrome and Related Disorders 17(10):505-511 (2019)
Allele C
OR 0.05
p 5.0e-14
N 291,107
Major Consortium StudyLarge GWAS
European

cholesterol to total lipids in medium LDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.01
p 9.0e-12
N 450,015
Large GWAS
multi-ancestry

free cholesterol to total lipids in 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 C
OR 0.01
p 2.0e-10
N 450,015
Large GWAS
multi-ancestry

type 2 diabetes mellitus

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.07
p 6.0e-10
N 667,504
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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