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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYLD-AS2, CYLD
(K767* +3 more)
Single nucleotide variant
(nonsense +1 more)
Familial cylindromatosis
+2 more
GPathogenic
CYLD, CYLD-AS2
(C684fs +3 more)
Duplication
(frameshift variant +1 more)
Brooke-Spiegler syndrome
GLikely pathogenic