rs9982601
▶GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (4)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
myocardial infarction
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 0.10
p 1.0e-20
N 315,668
Major Consortium StudyLarge GWAS
European
Kathiresan S et al. “Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.” Nature Genetics 41(3):334-41 (2009)
Allele T
OR 1.20
p 6.0e-11
N 6,042
Large GWAS
European
Wakil SM et al. “A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.” Atherosclerosis 245:62-70 (2016)
Allele T
OR 1.38
p 2.0e-13
N 4,431
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)
coronary artery disease
Dichgans M et al. “Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.” Stroke 45(1):24-36 (2014)
Allele T
OR 1.18
p 3.0e-10
N 109,124
Large GWAS
Schunkert H et al. “Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.” Nature Genetics 43(4):333-338 (2011)
Allele T
OR 1.18
p 4.0e-10
N 86,995
Large GWAS
European
drug use measurement, myocardial infarction
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 C
OR 0.09
p 2.0e-13
N 404,034
Major Consortium StudyLarge GWAS
multi-ancestry
pulse pressure measurement
Surendran P et al. “Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.” Nature Genetics 52(12):1314-1332 (2020)
Allele T
OR 0.19
p 4.0e-12
N 810,865
Meta-analysisLarge 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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