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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXP2
(R513fs +3 more)
Deletion
(frameshift variant +1 more)
Childhood apraxia of speech
GPathogenic
FOXP2
(H462R +4 more)
Single nucleotide variant
(missense variant +1 more)
Childhood apraxia of speech
GUncertain significance