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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PHOX2B
Duplication
(inframe_insertion)
not provided
+3 more
GPathogenic
RET
(C618G +12 more)
Single nucleotide variant
(missense variant)
Familial medullary thyroid carcinoma
+8 more
GPathogenic