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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NIPBL
(R1147*)
Single nucleotide variant
(nonsense)
De Lange syndrome
GPathogenic
NIPBL
(R1828Q)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 1
GConflicting classifications of pathogenicity