"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CDON"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 303509	NM_001378964.1(CDON):c.1851+14G>A	CDON	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1476989	NM_001378964.1(CDON):c.620G>A (p.Gly207Asp)	CDON (G207D)	Single nucleotide variant (missense variant)	Holoprosencephaly 11	GUncertain significance
Select item 878004	NM_001378964.1(CDON):c.350-11A>G	CDON	Single nucleotide variant (intron variant)	Holoprosencephaly 11	GBenign/Likely benign

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