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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSD1
(Q236H)
Single nucleotide variant
(missense variant +1 more)
Sotos syndrome
+1 more
GBenign/Likely benign
NSD1
(D1103N +4 more)
Single nucleotide variant
(missense variant)
Sotos syndrome
+1 more
GBenign/Likely benign
NSD1
(C1640S +5 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
NSD1
(G2585R +6 more)
Single nucleotide variant
(missense variant)
Sotos syndrome
+1 more
GConflicting classifications of pathogenicity
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