RS201853168 CYP4F22

Health Risk Chr 19:15551406
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CYP4F22
rs118203935 rs118203936 rs118203937 rs531800013 rs146026019 rs202078702 rs150739429 rs371097842 rs148977089 rs374106918
Ask Dr. Hemsworth about this variant