RS1064792878 TYMP

Health Risk Chr 22:50526000
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial DNA depletion syndrome 1
Inborn genetic diseases
Mitochondrial neurogastrointestinal encephalomyopathy
Mitochondrial DNA depletion syndrome 1
Inborn genetic diseases
Mitochondrial neurogastrointestinal encephalomyopathy
Other Variants in TYMP
rs121913036 rs797044454 rs121913037 rs149977726 rs786205097 rs797044455 rs786205098 rs121913038 rs28931613 rs767245071
Ask Dr. Hemsworth about this variant