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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD2
(E921del +1 more)
Microsatellite
(inframe_deletion +1 more)
Autistic behavior
GUncertain significance
SETD2
(S300N +1 more)
Single nucleotide variant
(missense variant +1 more)
Luscan-Lumish syndrome
+1 more
GUncertain significance