chorioretinal abnormality Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the choroid and retina. (Human Phenotype Ontology, HP_0000532)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0000532
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Genes

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

Symbol Name Standardized Value
RASIP1 Ras interacting protein 1 1.58913
LINC00461 long intergenic non-protein coding RNA 461 1.20542
ATXN2 ataxin 2 1.09351
SRSF2 serine/arginine-rich splicing factor 2 0.808951
FLT1 fms-related tyrosine kinase 1 0.4246
MFSD11 major facilitator superfamily domain containing 11 0.396616