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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD2
(D1938fs +1 more)
Duplication
(frameshift variant +1 more)
Luscan-Lumish syndrome
GPathogenic
SETD2
(G14V +1 more)
Single nucleotide variant
(missense variant +1 more)
Luscan-Lumish syndrome
GUncertain significance