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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECP2
(A140V +2 more)
Single nucleotide variant
(missense variant +1 more)
Autism, susceptibility to, X-linked 3
+15 more
GPathogenic/Likely pathogenic
MECP2
(E38fs +1 more)
Deletion
(frameshift variant +1 more)
Bulbar palsy
+11 more
GLikely pathogenic