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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXP2
(Q168H +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely pathogenic
FOXP2
(Q169* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GLikely pathogenic
FOXP2
(Q186* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
FOXP2
(R328* +3 more)
Single nucleotide variant
(nonsense +1 more)
Inborn genetic diseases
+2 more
GPathogenic
FOXP2
(N499fs +3 more)
Deletion
(frameshift variant +1 more)
not provided
GPathogenic
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