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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130002133, PTCH1
(A23D)
Single nucleotide variant
(missense variant +2 more)
Basal cell carcinoma, susceptibility to, 1
GUncertain significance
LOC130002133, PTCH1
(R13C)
Single nucleotide variant
(missense variant +2 more)
Basal cell carcinoma, susceptibility to, 1
+2 more
GUncertain significance