chromosomal disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A genetic disease that has_material_basis_in extra, missing, or re-arranged chromosomes. (Human Disease Ontology, DOID_0080014)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0080014
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Genes

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

Symbol Name Standardized Value
EPHB2 EPH receptor B2 0.746396
TGFBR3 transforming growth factor, beta receptor III 0.601018
BMP6 bone morphogenetic protein 6 0.540459