RS201233398 AMT

Health Risk Chr 3:49420219
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Associated Conditions
Glycine encephalopathy
Inborn genetic diseases
Glycine encephalopathy
Inborn genetic diseases
Other Variants in AMT
rs121964981 rs121964982 rs121964983 rs121964984 rs121964985 rs121964986 rs181134220 rs386833677 rs386833678 rs386833679
Ask Dr. Hemsworth about this variant