"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126862 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2629058	NM_001372.4(DNAH9):c.2928+1G>A	DNAH9, LOC126862505	Single nucleotide variant (splice donor variant)	DNAH9-related disorder +1 more	GLikely pathogenic
Select item 780399	NM_001372.4(DNAH9):c.2969G>A (p.Arg990His)	DNAH9, LOC126862505 (R990H)	Single nucleotide variant (missense variant)	DNAH9-related disorder +1 more	GBenign
Select item 1065498	NM_001372.4(DNAH9):c.2984del (p.Arg995fs)	DNAH9, LOC126862505 (R995fs)	Deletion (frameshift variant)	Non-immune hydrops fetalis +2 more	GPathogenic
Select item 1597197	NM_001372.4(DNAH9):c.3003C>A (p.Gly1001=)	DNAH9, LOC126862505	Single nucleotide variant (synonymous variant)	DNAH9-related disorder +1 more	GBenign
Select item 770639	NM_001372.4(DNAH9):c.3050A>G (p.Tyr1017Cys)	DNAH9, LOC126862505 (Y1017C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2421163	NM_001372.4(DNAH9):c.3186C>T (p.Ile1062=)	DNAH9, LOC126862505	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

ClinVar