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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZMIZ1
(G868S)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies
+1 more
GUncertain significance
ZMIZ1
(P873S)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies
GUncertain significance