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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(K666N +14 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia type 2A
+7 more
GPathogenic/Likely pathogenic
RET
(K412N +13 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GPathogenic/Likely pathogenic