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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KAT6B
(E1075* +7 more)
Single nucleotide variant
(nonsense)
Blepharophimosis - intellectual disability syndrome, SBBYS type
GPathogenic
KAT6B
(E1681K +7 more)
Single nucleotide variant
(missense variant)
Developmental disorder
+1 more
GLikely pathogenic