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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KANSL1
(S993I +1 more)
Single nucleotide variant
(missense variant)
Developmental disorder
GLikely benign
KANSL1
(V589M)
Single nucleotide variant
(missense variant)
Neurodevelopmental abnormality
GLikely benign