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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYLD
(L152fs)
Deletion
(frameshift variant +2 more)
not provided
GLikely pathogenic
CYLD
(A156V +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance