C4749028[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1355800	NM_001372.4(DNAH9):c.2584G>T (p.Ala862Ser)	DNAH9 (A862S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1333258	NM_001372.4(DNAH9):c.6669G>A (p.Trp2223Ter)	DNAH9 (W2223*)	Single nucleotide variant (nonsense)	Ciliary dyskinesia, primary, 40	GLikely pathogenic
Select item 1436443	NM_001372.4(DNAH9):c.8893C>T (p.Arg2965Cys)	DNAH9 (R2965C)	Single nucleotide variant (missense variant)	Ciliary dyskinesia, primary, 40 +1 more	GUncertain significance

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