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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSC2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
TSC2
(G440S +4 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
TSC2
(D1612N +9 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis 2
+2 more
GConflicting classifications of pathogenicity
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