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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTCH1
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PTCH1
(A247V +3 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity