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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRCAP
(V826fs)
Duplication
(frameshift variant)
Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities
GLikely pathogenic
SRCAP
(R2444*)
Single nucleotide variant
(nonsense)
Floating-Harbor syndrome
+5 more
GPathogenic