"PreventionGenetics, part of Exact Sciences"[submitter] AND "NOX1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 727642	NM_007052.5(NOX1):c.1278C>G (p.His426Gln)	NOX1 (H389Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3056188	NM_007052.5(NOX1):c.1237A>G (p.Ile413Val)	NOX1 (I376V +1 more)	Single nucleotide variant (missense variant)	NOX1-related disorder	GLikely benign
Select item 791381	NM_007052.5(NOX1):c.1133G>A (p.Arg378Lys)	NOX1 (R378K +1 more)	Single nucleotide variant (missense variant)	NOX1-related disorder +1 more	GBenign
Select item 720642	NM_007052.5(NOX1):c.765C>T (p.Ser255=)	NOX1	Single nucleotide variant (synonymous variant)	NOX1-related disorder +1 more	GBenign
Select item 3048539	NM_007052.5(NOX1):c.340A>G (p.Ile114Val)	NOX1 (I114V +1 more)	Single nucleotide variant (missense variant)	NOX1-related disorder	GBenign
Select item 3045157	NM_007052.5(NOX1):c.142-4G>A	NOX1	Single nucleotide variant (intron variant)	NOX1-related disorder	GLikely benign

ClinVar