rs2019090

GWAS Catalog Trait Associations (6)

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

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 A
OR 0.06
p 1.0e-30
N 424,341
Major Consortium StudyLarge GWAS
European

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 A
OR 0.06
p 2.0e-30
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 A
OR 0.06
p 2.0e-23
N 429,794
Major Consortium StudyLarge GWAS
European

drug use measurement, 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 A
OR 0.07
p 3.0e-21
N 315,668
Major Consortium StudyLarge GWAS
European

myocardial infarction

Hartiala JA et al. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. European Heart Journal 42(9):919-933 (2021)
Allele A
OR 1.07
p 2.0e-18
N 639,221
Large GWAS
multi-ancestry
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 A
OR 0.05
p 3.0e-11
N 432,053
Major Consortium StudyLarge GWAS
European
Allele A
OR 1.07
p 4.0e-9
N 166,459
Meta-analysisLarge GWAS
multi-ancestry

carotid artery thickness

Allele A
OR 0.04
p 1.0e-9
N 45,185
Meta-analysisLarge GWAS
multi-ancestry
Allele A
OR 0.01
p 8.0e-9
N 22,179
Major Consortium StudyLarge 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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