"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CCDC22"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1032586	NM_014008.5(CCDC22):c.383G>A (p.Arg128Gln)	CCDC22 (R128Q)	Single nucleotide variant (missense variant)	Ritscher-Schinzel syndrome 2	GUncertain significance
Select item 210617	NM_014008.5(CCDC22):c.536-7C>T	CCDC22	Single nucleotide variant (intron variant)	Ritscher-Schinzel syndrome 2 +2 more	GBenign/Likely benign
Select item 1306352	NM_014008.5(CCDC22):c.1873C>T (p.Arg625Trp)	CCDC22 (R625W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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