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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC106736614, RET
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
LOC106736614, RET
(L11M)
Single nucleotide variant
(missense variant)
Multiple endocrine neoplasia, type 2
+3 more
GConflicting classifications of pathogenicity