rs6504213

GWAS Catalog Trait Associations (8)

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

systolic blood pressure

Allele C
OR 0.24
p 6.0e-22
N 1,028,980
Large GWAS
multi-ancestry
Allele C
OR 0.02
p 4.0e-20
N 1,212,859
Large GWAS
European
Allele C
OR 0.01
p 1.0e-12
N 394,642
Large GWAS
European

pulse pressure measurement

Allele C
OR 0.16
p 1.0e-19
N 1,028,980
Large GWAS
multi-ancestry
Allele C
OR 0.14
p 3.0e-8
N 459,777
Large GWAS
multi-ancestry

coronary artery disease

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.04
p 2.0e-18
N 417,274
Major Consortium StudyLarge GWAS
European

heart disease

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.04
p 4.0e-14
N 429,794
Major Consortium StudyLarge GWAS
European

essential hypertension

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.04
p 6.0e-12
N 427,704
Major Consortium StudyLarge GWAS
European

coronary atherosclerosis

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.04
p 7.0e-12
N 602,192
Major Consortium StudyLarge GWAS
multi-ancestry

diastolic blood pressure

Allele C
OR 0.10
p 9.0e-10
N 1,028,980
Large GWAS
multi-ancestry

platelet volume

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.03
p 3.0e-18
N 476,837
Major Consortium StudyLarge 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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