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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(K563fs +2 more)
Deletion
(frameshift variant)
Lynch syndrome 5
+4 more
GPathogenic
CTNNB1, LOC126806659
(R474* +1 more)
Single nucleotide variant
(nonsense)
Medulloblastoma
+11 more
GPathogenic