antiphospholipid syndrome Gene Set

Dataset	GWASdb SNP-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A hypersensitivity reaction type II disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin). (Human Disease Ontology, DOID_2988)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:2988
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Genes

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

Symbol	Name	Standardized Value
MYO16	myosin XVI	1.14463
MICAL3	microtubule associated monooxygenase, calponin and LIM domain containing 3	1.14463
PDE1C	phosphodiesterase 1C, calmodulin-dependent 70kDa	1.10764
EVA1A	eva-1 homolog A (C. elegans)	1.04846
DSTN	destrin (actin depolymerizing factor)	1.02476
MACROD2	MACRO domain containing 2	1.00407
SGIP1	SH3-domain GRB2-like (endophilin) interacting protein 1	1.00407