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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GFAP
(A233T)
Single nucleotide variant
(missense variant)
Alexander disease
GUncertain significance
GFAP
Single nucleotide variant
(splice acceptor variant)
Alexander disease
GUncertain significance
GFAP
(E72G)
Single nucleotide variant
(missense variant)
Alexander disease
GLikely pathogenic
GFAP
(R66Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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