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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTCH2
(L435P)
Indel
(missense variant)
Gorlin syndrome
+1 more
GPathogenic
PTCH2
(V433fs)
Indel
(frameshift variant)
Gorlin syndrome
GConflicting classifications of pathogenicity
PTCH2
(V433fs)
Deletion
(frameshift variant)
Basal cell carcinoma, susceptibility to, 1
+1 more
GConflicting classifications of pathogenicity
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