familial hypertriglyceridemia Gene Set

Dataset	GWASdb SNP-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A lipid metabolism disorder characterized by elevated triglyceride levels as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. (Human Disease Ontology, DOID_0050527)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0050527
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Genes

7 genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol	Name	Standardized Value
GCKR	glucokinase (hexokinase 4) regulator	1.7256
TMEM241	transmembrane protein 241	1.39396
TBL2	transducin (beta)-like 2	1.14463
HAVCR1	hepatitis A virus cellular receptor 1	1.10764
BAZ1B	bromodomain adjacent to zinc finger domain, 1B	1.10764
FAN1	FANCD2/FANCI-associated nuclease 1	1.02476
PHYHIP	phytanoyl-CoA 2-hydroxylase interacting protein	1.00407