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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECP2
(R133C +2 more)
Single nucleotide variant
(missense variant +1 more)
Rett syndrome
GPathogenic
MECP2
(S13* +1 more)
Single nucleotide variant
(nonsense +1 more)
Rett syndrome
+1 more
GPathogenic