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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC2A1
(G314S)
Single nucleotide variant
(missense variant)
GLUT1 deficiency syndrome 1, autosomal recessive
+3 more
GPathogenic
SLC2A1
(T295M)
Single nucleotide variant
(missense variant)
GLUT1 deficiency syndrome
+3 more
GPathogenic