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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLI2
(G49E)
Single nucleotide variant
(missense variant +1 more)
Holoprosencephaly 9
GUncertain significance
GLI2
(T13M +1 more)
Single nucleotide variant
(missense variant)
Holoprosencephaly 9
GConflicting classifications of pathogenicity
GLI2
(P889L +2 more)
Single nucleotide variant
(missense variant)
Holoprosencephaly 9
+1 more
GUncertain significance
GLI2
(Y1306H +2 more)
Single nucleotide variant
(missense variant)
Holoprosencephaly 9
GUncertain significance
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