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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(L17P)
Single nucleotide variant
(missense variant)
Family history of cancer
+2 more
GUncertain significance
PALB2
(V398fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic