esophagus squamous cell carcinoma Gene Set

Dataset	GWASdb SNP-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus. (Human Disease Ontology, DOID_3748)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:3748
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Genes

15 genes associated with the disease esophagus squamous cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol	Name	Standardized Value
APOE	apolipoprotein E	3.576
TOMM40	translocase of outer mitochondrial membrane 40 homolog (yeast)	2.39826
LPA	lipoprotein, Lp(a)	2.21675
LDLR	low density lipoprotein receptor	2.14896
DNAH11	dynein, axonemal, heavy chain 11	1.8787
LRFN2	leucine rich repeat and fibronectin type III domain containing 2	1.69467
HMGCR	3-hydroxy-3-methylglutaryl-CoA reductase	1.49655
ABCG8	ATP-binding cassette, sub-family G (WHITE), member 8	1.40698
SLCO1B1	solute carrier organic anion transporter family, member 1B1	1.34719
APOC1	apolipoprotein C-I	1.01598
FBXO11	F-box protein 11	0.774314
CETP	cholesteryl ester transfer protein, plasma	0.764084
ABCC2	ATP-binding cassette, sub-family C (CFTR/MRP), member 2	0.694381
PLCXD2	phosphatidylinositol-specific phospholipase C, X domain containing 2	0.636511
RELN	reelin	0.510444