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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RET
(C634G +14 more)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+4 more
GPathogenic
RET
(S891A +17 more)
Single nucleotide variant
(missense variant)
Hirschsprung disease, susceptibility to, 1
+10 more
GPathogenic