RS766376173 SLC2A1
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Associated Conditions
GLUT1 deficiency syndrome 1
autosomal recessive
Inborn genetic diseases
Dystonia 9
Hereditary cryohydrocytosis with reduced stomatin
Encephalopathy due to GLUT1 deficiency
Childhood onset GLUT1 deficiency syndrome 2
Parkinsonian disorder
Epilepsy
idiopathic generalized
susceptibility to
12
GLUT1 deficiency syndrome 1
autosomal recessive
Inborn genetic diseases
Other Variants in SLC2A1