RS551975117 TYMP

Health Risk Chr 22:50526006
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Associated Conditions
Mitochondrial neurogastrointestinal encephalomyopathy
Inborn genetic diseases
Mitochondrial neurogastrointestinal encephalomyopathy
Inborn genetic diseases
Other Variants in TYMP
rs121913036 rs797044454 rs121913037 rs149977726 rs786205097 rs797044455 rs786205098 rs121913038 rs28931613 rs767245071
Ask Dr. Hemsworth about this variant