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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXP1
(P466A +4 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability
+4 more
GLikely pathogenic
ASXL1
(R404* +1 more)
Single nucleotide variant
(nonsense)
dystrophia
+14 more
GPathogenic