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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDON
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
CDON
(G207D)
Single nucleotide variant
(missense variant)
Holoprosencephaly 11
GUncertain significance
CDON
Single nucleotide variant
(intron variant)
Holoprosencephaly 11
GBenign/Likely benign
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