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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZMIZ1
(S140P)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies
GUncertain significance
ZMIZ1
(F378fs)
Duplication
(frameshift variant)
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies
GLikely pathogenic