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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSC2
(E371Q +8 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
TSC2
(S1097R +34 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance