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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EZH2
(N322S +3 more)
Single nucleotide variant
(missense variant)
Weaver syndrome
GConflicting classifications of pathogenicity
EZH2
Deletion
(intron variant)
not provided
+2 more
GBenign
EZH2
Deletion
(intron variant)
Weaver syndrome
GLikely benign
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