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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NIPBL
(A1308V)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 1
GUncertain significance
NIPBL
(Q2232E)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 1
GUncertain significance
NIPBL
(G2351del)
Deletion
(inframe deletion)
Cornelia de Lange syndrome 1
GUncertain significance
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