rs605066

This is a intergenic variant variant.

GWAS Catalog Trait Associations (9)

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

BMI-adjusted waist-hip ratio

Allele T
OR 0.02
p 3.0e-40
N 379,501
Meta-analysisLarge GWAS
European

phospholipids in chylomicrons and extremely large VLDL 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 0.04
p 1.0e-38
N 241,027
Large GWAS
European

concentration of chylomicrons and extremely large VLDL particles 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 0.04
p 4.0e-37
N 241,027
Large GWAS
European

waist-hip ratio

Allele T
OR 0.02
p 2.0e-26
N 697,734
Meta-analysisLarge GWAS
European

HDL particle size

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-26
N 450,015
Large GWAS
multi-ancestry

non-alcoholic fatty liver disease

Allele C
OR 0.04
p 1.0e-18
N 122,644
Large GWAS
European

diastolic blood pressure

Allele T
OR 0.11
p 6.0e-10
N 810,865
Meta-analysisLarge GWAS
European

high density lipoprotein cholesterol measurement

Allele C
OR 0.01
p 4.0e-8
N 133,824
Large GWAS
multi-ancestry
Allele C
OR 0.39
p 3.0e-8
N 99,900
Large GWAS
European
Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.026
p 6.0e-12
N 94,674
Large GWAS
multi-ancestry
Willer CJ et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics 45(11):1274-1283 (2013)
Allele C
OR
β 0.028
p 3.0e-8
N 94,595
Large GWAS
European

triglyceride measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.030
p 9.0e-13
N 94,674
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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