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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POGZ
(R1087* +4 more)
Single nucleotide variant
(nonsense)
See cases
+2 more
GPathogenic/Likely pathogenic
POGZ
(R784* +4 more)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
POGZ
(M332fs +4 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder
+5 more
GPathogenic
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