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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD2
(R1950K +1 more)
Single nucleotide variant
(missense variant +1 more)
Luscan-Lumish syndrome
GUncertain significance
SETD2
(R1268G +1 more)
Single nucleotide variant
(missense variant +1 more)
Luscan-Lumish syndrome
GUncertain significance
SETD2
(S816I +1 more)
Single nucleotide variant
(missense variant +1 more)
Luscan-Lumish syndrome
GUncertain significance
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