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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAD21
Deletion
(intron variant)
Cornelia de Lange syndrome 4
+2 more
GBenign/Likely benign
RAD21
Single nucleotide variant
(splice acceptor variant)
not specified
+3 more
GLikely benign