RS181134220 AMT

Health Risk Chr 3:49417974
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What This Variant Does
"CLNSIG=5
Associated Conditions
Glycine encephalopathy
Glycine encephalopathy 2
Glycine encephalopathy 1
Inborn genetic diseases
Glycine encephalopathy
Glycine encephalopathy 2
Glycine encephalopathy 1
Inborn genetic diseases
Other Variants in AMT
rs121964981 rs121964982 rs121964983 rs121964984 rs121964985 rs121964986 rs386833677 rs386833678 rs386833679 rs386833680
Ask Dr. Hemsworth about this variant