RS80359819 SLC2A1

Health Risk Chr 1:42930754
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
GLUT1 deficiency syndrome
GLUT1 deficiency syndrome 1
autosomal recessive
Encephalopathy due to GLUT1 deficiency
GLUT1 deficiency syndrome 1
autosomal recessive
Inborn genetic diseases
GLUT1 deficiency syndrome
GLUT1 deficiency syndrome 1
autosomal recessive
Encephalopathy due to GLUT1 deficiency
GLUT1 deficiency syndrome 1
autosomal recessive
Other Variants in SLC2A1
rs80359829 rs80359828 rs80359816 rs80359814 rs2124448824 rs121909739 rs121909740 rs80359812 rs267607060 rs267607061
Ask Dr. Hemsworth about this variant