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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR26
Single nucleotide variant
(splice donor variant)
Skraban-Deardorff syndrome
GPathogenic
WDR26
(R233C +2 more)
Single nucleotide variant
(missense variant)
Skraban-Deardorff syndrome
GUncertain significance
WDR26
(N246H +2 more)
Single nucleotide variant
(missense variant)
Skraban-Deardorff syndrome
GUncertain significance
CNIH3, CNIH4
+5 more
Copy number loss
not provided
GPathogenic
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