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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLI3
(P1548S)
Single nucleotide variant
(missense variant)
Pallister-Hall syndrome
GUncertain significance
GLI3
(R792*)
Single nucleotide variant
(nonsense)
Polydactyly, postaxial, type A1
+3 more
GPathogenic