rs180803

This is a intron variant variant in the POM121L9P gene.

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GWAS Catalog Trait Associations (2)

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

coronary artery disease

Nikpay M et al. “A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.” Nature Genetics 47(10):1121-1130 (2015)

Allele G

OR 1.20

p 2.0e-10

N 187,599

Meta-analysisLarge GWAS

multi-ancestry

Nelson CP et al. “Association analyses based on false discovery rate implicate new loci for coronary artery disease.” Nature Genetics 49(9):1385-1391 (2017)

Allele G

OR 1.18

p 7.0e-10

N 63,731

Large GWAS

European, NR

myocardial infarction

Nikpay M et al. “A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.” Nature Genetics 47(10):1121-1130 (2015)

Allele G

OR 1.21

p 4.0e-9

N 166,459

Meta-analysisLarge GWAS

multi-ancestry

Hartiala JA et al. “Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.” European Heart Journal 42(9):919-933 (2021)

Allele G

OR 1.16

p 2.0e-8

N 639,221

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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