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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDON
(S1130N)
Single nucleotide variant
(missense variant)
Holoprosencephaly 11
GUncertain significance
CDON
(N746fs)
Deletion
(frameshift variant)
Holoprosencephaly 11
GUncertain significance
CDON
(P607S)
Single nucleotide variant
(missense variant)
Holoprosencephaly 11
GUncertain significance
CDON
(P3S)
Single nucleotide variant
(missense variant)
Holoprosencephaly 11
+1 more
GUncertain significance
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