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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDC42BPB
(E920fs)
Microsatellite
(frameshift variant)
Chilton-Okur-Chung neurodevelopmental syndrome
GLikely pathogenic
CDC42BPB
(R626G)
Single nucleotide variant
(missense variant)
Chilton-Okur-Chung neurodevelopmental syndrome
GUncertain significance