aortic disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An artery disease that is characterized by degeneration of the cells composing the aortic wall. (Human Disease Ontology, DOID_520)
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16 genes associated with the disease aortic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
FBN1 fibrillin 1 1.21253
LDLR low density lipoprotein receptor 0.919371
SLC30A8 solute carrier family 30 (zinc transporter), member 8 0.911235
LRP1 low density lipoprotein receptor-related protein 1 0.867193
DAB2IP DAB2 interacting protein 0.867193
CDKN2B-AS1 CDKN2B antisense RNA 1 0.638262
TDRD10 tudor domain containing 10 0.468527
MPPED2 metallophosphoesterase domain containing 2 0.462668
GPC6 glypican 6 0.462055
KCNIP3 Kv channel interacting protein 3, calsenilin 0.448948
RORA RAR-related orphan receptor A 0.44876
IL6R interleukin 6 receptor 0.445287
PGR progesterone receptor 0.44062
MYT1L myelin transcription factor 1-like 0.420588
ZNF665 zinc finger protein 665 0.416702
BMP4 bone morphogenetic protein 4 0.415804