rs2378335
This variant is located in the MMP24-AS1-EDEM2 gene.
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Thromboembolism
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 0.12
p 2.0e-33
N 438,632
Major Consortium StudyLarge GWAS
European
pulmonary embolism, Pulmonary 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 A
OR 0.12
p 5.0e-17
N 447,859
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 0.12
p 8.0e-17
N 447,635
Major Consortium StudyLarge GWAS
European
deep vein thrombosis
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 0.13
p 3.0e-18
N 400,487
Major Consortium StudyLarge GWAS
multi-ancestry
drug use measurement, deep vein thrombosis
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 0.14
p 7.0e-17
N 400,487
Major Consortium StudyLarge GWAS
multi-ancestry
About MMP24-AS1-EDEM2
This record represents naturally-occurring readthrough transcription between upstream GeneID:101410538 (MMP24 antisense RNA 1) and the ER degradation enhancing alpha-mannosidase like protein 2 (EDEM2) gene. Readthrough transcripts may encode proteins similar to those encoded by the EDEM2 gene. [provided by RefSeq, Aug 2017]
View all MMP24-AS1-EDEM2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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