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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMC3
(W473G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SMC3
(M648V)
Single nucleotide variant
(missense variant)
Intellectual disability
+2 more
GPathogenic/Likely pathogenic
SMC3
(K673R)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(K838T)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GLikely pathogenic
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