aortic aneurysm Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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 aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
FBN1 fibrillin 1 1.57861
LDLR low density lipoprotein receptor 0.808951
SLC30A8 solute carrier family 30 (zinc transporter), member 8 0.801423
LRP1 low density lipoprotein receptor-related protein 1 0.760549
DAB2IP DAB2 interacting protein 0.760549
CDKN2B-AS1 CDKN2B antisense RNA 1 0.542759
TDRD10 tudor domain containing 10 0.400228
MPPED2 metallophosphoesterase domain containing 2 0.395376
GPC6 glypican 6 0.3949
KCNIP3 Kv channel interacting protein 3, calsenilin 0.384313
RORA RAR-related orphan receptor A 0.384177
IL6R interleukin 6 receptor 0.381605
PGR progesterone receptor 0.378089
MYT1L myelin transcription factor 1-like 0.36355
ZNF665 zinc finger protein 665 0.360702
BMP4 bone morphogenetic protein 4 0.360105