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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARID1B
Insertion
(inframe_insertion)
Coffin-Siris syndrome
GUncertain significance
SMARCA4
(P195H)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 16
+2 more
GUncertain significance