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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLI2
(R772W +2 more)
Single nucleotide variant
(missense variant)
Holoprosencephaly 9
GUncertain significance
GLI2
(R1526C +2 more)
Single nucleotide variant
(missense variant)
Microcephaly
GUncertain significance