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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLI3
(E490*)
Single nucleotide variant
(nonsense)
Greig cephalopolysyndactyly syndrome
GPathogenic
GLI3
(D170H)
Single nucleotide variant
(missense variant)
Greig cephalopolysyndactyly syndrome
GUncertain significance