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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLI3
(L1479S)
Single nucleotide variant
(missense variant)
Cronkhite-Canada syndrome
GUncertain significance
GLI3
(R667L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+9 more
GUncertain significance