RS796053248 SLC2A1
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What This Variant Does
"CLNSIG=5
Associated Conditions
GLUT1 deficiency syndrome 1
autosomal recessive
Dystonia 9
Epilepsy
idiopathic generalized
susceptibility to
12
Encephalopathy due to GLUT1 deficiency
Childhood onset GLUT1 deficiency syndrome 2
Hereditary cryohydrocytosis with reduced stomatin
GLUT1 deficiency syndrome 1
autosomal recessive
Dystonia 9
Epilepsy
idiopathic generalized
Other Variants in SLC2A1