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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SYNCRIP
(D3fs +2 more)
Duplication
(frameshift variant)
SYNCRIP-associated neurodevelopmental disorder
GLikely pathogenic
SNX14, SYNCRIP
Copy number loss
SYNCRIP-associated neurodevelopmental disorder
GLikely pathogenic