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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTCH1
(A788G +4 more)
Single nucleotide variant
(missense variant +1 more)
Gorlin syndrome
GUncertain significance
SUFU
(T353M)
Single nucleotide variant
(missense variant)
Familial meningioma
+4 more
GConflicting classifications of pathogenicity