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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTCH1
(Q262* +3 more)
Single nucleotide variant
(nonsense +1 more)
Medulloblastoma
+1 more
GPathogenic
PTCH1
Single nucleotide variant
(intron variant)
Congenital omphalocele
GUncertain significance