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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSD2
(E650fs)
Deletion
(frameshift variant)
Rauch-Steindl syndrome
GPathogenic
NSD2
(R892K)
Single nucleotide variant
(missense variant)
4p partial monosomy syndrome
GUncertain significance
NSD2
(E1099K)
Single nucleotide variant
(missense variant)
Anemia
+14 more
GConflicting classifications of pathogenicity
NSD2
(R1138G)
Single nucleotide variant
(missense variant)
Rauch-Steindl syndrome
GUncertain significance
NSD2
(E1279fs)
Deletion
(frameshift variant)
Rauch-Steindl syndrome
GLikely pathogenic
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