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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC2A1
(L284P)
Single nucleotide variant
(missense variant)
Childhood onset GLUT1 deficiency syndrome 2
GLikely pathogenic
SLC2A1
(E246fs)
Microsatellite
(frameshift variant)
Encephalopathy due to GLUT1 deficiency
+2 more
GPathogenic