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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TET3
(I802fs +1 more)
Deletion
(frameshift variant)
Beck-Fahrner syndrome
GLikely pathogenic
TET3
(H1592fs +1 more)
Duplication
(frameshift variant)
Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
GUncertain significance