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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130002132, PTCH1
Single nucleotide variant
(intron variant)
Gorlin syndrome
+1 more
GLikely benign
LOC130002132, PTCH1
Single nucleotide variant
(intron variant)
Gorlin syndrome
+1 more
GConflicting classifications of pathogenicity