RS80359818 SLC2A1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Encephalopathy due to GLUT1 deficiency
Childhood onset GLUT1 deficiency syndrome 2
Dystonia 9
GLUT1 deficiency syndrome 1
autosomal recessive
Hereditary cryohydrocytosis with reduced stomatin
Chromosome 17q23.1-q23.2 deletion syndrome
SLC2A1-related disorder
Inborn genetic diseases
Encephalopathy due to GLUT1 deficiency
Childhood onset GLUT1 deficiency syndrome 2
Dystonia 9
GLUT1 deficiency syndrome 1
autosomal recessive
Hereditary cryohydrocytosis with reduced stomatin
Other Variants in SLC2A1