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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNNB1, LOC126806659
(Q482* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
CTNNB1, LOC126806659
(H492fs +1 more)
Duplication
(frameshift variant)
not provided
+1 more
GPathogenic
CTNNB1
(M688V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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