abnormality of the retinal vasculature Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An arterial or venous retinal vascular anomaly. (Human Phenotype Ontology, HP_0008046)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0008046
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Genes

6 genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
RASIP1 Ras interacting protein 1 1.58913
SRSF2 serine/arginine-rich splicing factor 2 1.41863
LINC00461 long intergenic non-protein coding RNA 461 1.20542
ATXN2 ataxin 2 1.09351
FLT1 fms-related tyrosine kinase 1 1.0453
MFSD11 major facilitator superfamily domain containing 11 0.786