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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECP2
(L293fs +2 more)
Deletion
(frameshift variant)
Rett syndrome
+2 more
GPathogenic
MECP2
Single nucleotide variant
(synonymous variant +1 more)
Rett syndrome
+2 more
GPathogenic