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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD2
(S2194fs +1 more)
Deletion
(frameshift variant +1 more)
Luscan-Lumish syndrome
GPathogenic
SETD2
(D1797fs +1 more)
Microsatellite
(frameshift variant +1 more)
Luscan-Lumish syndrome
GLikely pathogenic
SETD2
(E27Q)
Single nucleotide variant
(missense variant +2 more)
Rabin-Pappas syndrome
+3 more
GConflicting classifications of pathogenicity
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