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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSD1
(S716fs +1 more)
Microsatellite
(frameshift variant)
not provided
+3 more
GPathogenic
NSD1
(A2383del +6 more)
Microsatellite
(inframe_indel +1 more)
Abnormal cerebral morphology
GUncertain significance