rs7246865

GWAS Catalog Trait Associations (10)

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

diastolic blood pressure

Allele A
OR 0.19
p 7.0e-28
N 1,028,980
Large GWAS
multi-ancestry
Allele A
OR 0.01
p 1.0e-19
N 928,679
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 A
OR 0.02
p 4.0e-12
N 485,677
Large GWAS
multi-ancestry

systolic blood pressure

Allele A
OR 0.29
p 5.0e-26
N 1,028,980
Large GWAS
multi-ancestry
Allele A
OR 0.02
p 2.0e-15
N 1,212,859
Large GWAS
European
Allele A
OR 0.01
p 6.0e-17
N 928,679
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 A
OR 0.01
p 8.0e-11
N 485,664
Large GWAS
multi-ancestry

appendicular lean mass

Allele A
OR 0.02
p 1.0e-21
N 450,243
Major Consortium StudyLarge GWAS
European

hypertension

Allele A
OR 0.05
p 3.0e-16
N 394,626
Large GWAS
European

Agents acting on the renin-angiotensin system use measurement

Allele A
OR 0.05
p 7.0e-13
N 237,530
Major Consortium StudyLarge GWAS
European

mean arterial pressure

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele A
OR 0.01
p 2.0e-12
N 506,365
Large GWAS
multi-ancestry

cholesterol to total lipids in large VLDL 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 4.0e-11
N 450,015
Large GWAS
multi-ancestry

coronary artery disease

Allele A
OR 1.03
p 2.0e-8
N 1,165,690
Large GWAS
European, NR
Allele A
OR 1.03
p 4.0e-8
N 773,268
Large GWAS
European

reticulocyte count

Allele A
OR 0.02
p 4.0e-9
N 170,690
Large GWAS
European

Abnormality of the skeletal system

Allele A
OR 0.01
p 6.0e-16
N 394,642
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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