RS750707642 TYMP

Health Risk Chr 22:50526630
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in TYMP
rs121913036 rs797044454 rs121913037 rs149977726 rs786205097 rs797044455 rs786205098 rs121913038 rs28931613 rs767245071
Ask Dr. Hemsworth about this variant