rs2895811

This variant is located in the HHIPL1 gene.

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GWAS Catalog Trait Associations (1)

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

coronary artery disease

van der Harst P et al. “Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.” Circulation Research 122(3):433-443 (2018)

Allele C

OR 0.04

p 1.0e-14

N 250,736

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 C

OR 1.07

p 1.0e-10

N 86,995

Large GWAS

European

About HHIPL1

This gene encodes a protein that belongs to the glucose/sorbosone dehydrogenase family. The encoded protein also contains a domain that binds folate and reduced folic acid derivatives. [provided by RefSeq, Jul 2016]

View all HHIPL1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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