RS121964982 AMT

Health Risk Chr 3:49422223
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What This Variant Does
"[OMIM:?]
Associated Conditions
Glycine encephalopathy
Inborn genetic diseases
Glycine encephalopathy 1
Glycine encephalopathy 2
Glycine encephalopathy
Glycine encephalopathy
Inborn genetic diseases
Glycine encephalopathy 1
Glycine encephalopathy 2
Glycine encephalopathy
Other Variants in AMT
rs121964981 rs121964983 rs121964984 rs121964985 rs121964986 rs181134220 rs386833677 rs386833678 rs386833679 rs386833680
Ask Dr. Hemsworth about this variant