RS387907313 SLC2A1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Epilepsy
idiopathic generalized
susceptibility to
12
GLUT1 deficiency syndrome 1
autosomal recessive
Encephalopathy due to GLUT1 deficiency
Epilepsy
idiopathic generalized
susceptibility to
12
GLUT1 deficiency syndrome 1
autosomal recessive
Encephalopathy due to GLUT1 deficiency
Other Variants in SLC2A1