RS140786333 OAT

Health Risk Chr 10:124412065
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Associated Conditions
Ornithine aminotransferase deficiency
Inborn genetic diseases
OAT-related disorder
Ornithine aminotransferase deficiency
Inborn genetic diseases
OAT-related disorder
Other Variants in OAT
rs121965034 rs386833599 rs121965035 rs121965036 rs121965037 rs121965038 rs121965039 rs121965040 rs121965041 rs121965042
Ask Dr. Hemsworth about this variant