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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NIPBL
(K2767E)
Single nucleotide variant
(3 prime UTR variant +1 more)
Cornelia de Lange syndrome 1
GUncertain significance
NIPBL
(L2795P)
Single nucleotide variant
(3 prime UTR variant +1 more)
Cornelia de Lange syndrome 1
GLikely pathogenic