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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSC1
(G1000R +15 more)
Single nucleotide variant
(missense variant +1 more)
Tuberous sclerosis 1
GUncertain significance
TSC1
(V895I +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
TSC1
(T523A +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
TSC1
(R316Q +2 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis syndrome
+3 more
GConflicting classifications of pathogenicity
TSC1
(T300I +2 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis 1
+2 more
GConflicting classifications of pathogenicity
TSC1
(M142T +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
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