aortic aneurysm Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An aortic disease that is characterized by an enlargement (dilation) of the aorta to greater than 1.5 times normal size. (Human Disease Ontology, DOID_3627)
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16 genes associated with the disease aortic aneurysm 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