multiple mitochondrial dna deletions Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of multiple deletions of mitochondrial DNA (mtDNA). (Human Phenotype Ontology, HP_0003689)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0003689
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Genes

1 genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10 2.06978