OAT, ornithine aminotransferase, 4942

N. diseases: 92; N. variants: 71
Disease: Gyrate Atrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554867698
rs1554867698
Entrez Id: 4942
Gene Symbol: OAT
OAT
CUI: C0018425
Disease:
Gyrate Atrophy 		TTAA 0.700 GeneticVariation CLINVAR