abnormality of the cerebrospinal fluid Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the cerebrospinal fluid (CSF). (Human Phenotype Ontology, HP_0002921)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002921
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Genes

3 genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 1.32793
RPSAP52 ribosomal protein SA pseudogene 52 1.11203
TOMM40 translocase of outer mitochondrial membrane 40 homolog (yeast) 1.11203