rs2477088
This variant is located in the PDE4DIP gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
macrovascular complications of diabetes
Ustinova M et al. “Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia.” Bmc Medical Genomics 14(1):18 (2021)
Allele T
OR 2.50
p 6.0e-10
N 559
Small GWAS
European
About PDE4DIP
The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]
View all PDE4DIP variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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