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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD2
(E921del +1 more)
Microsatellite
(inframe_deletion +1 more)
Autistic behavior
GUncertain significance
KMT2C
(I1806V)
Single nucleotide variant
(missense variant)
Autistic behavior
GUncertain significance
KMT2C
(E1640Q)
Single nucleotide variant
(missense variant)
Kleefstra syndrome 2
+1 more
GUncertain significance
CHD3
(P1882L +2 more)
Single nucleotide variant
(missense variant)
Autistic behavior
GUncertain significance
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