RS80359826 SLC2A1
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What This Variant Does
"CLNSIG=5
Associated Conditions
GLUT1 deficiency syndrome 1
autosomal recessive
Epilepsy
Microcephaly
intellectual deficiency
Inborn genetic diseases
Encephalopathy due to GLUT1 deficiency
Childhood onset GLUT1 deficiency syndrome 2
Dystonia 9
Hereditary cryohydrocytosis with reduced stomatin
GLUT1 deficiency syndrome 1
autosomal recessive
Epilepsy
Microcephaly
intellectual deficiency
Other Variants in SLC2A1