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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSD2
(Q963*)
Single nucleotide variant
(nonsense)
4p partial monosomy syndrome
GPathogenic
NSD2
(G1162S)
Single nucleotide variant
(missense variant)
Rauch-Steindl syndrome
GLikely pathogenic
HAUS3, FAM53A
+16 more
Copy number loss
4p partial monosomy syndrome
GPathogenic
JAKMIP1, KIAA0232
+90 more
Copy number loss
4p partial monosomy syndrome
GPathogenic
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