"PreventionGenetics, part of Exact Sciences"[submitter] AND "DUOX1"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3038463	NM_175940.3(DUOX1):c.143-3C>A	DUOX1	Single nucleotide variant (intron variant)	DUOX1-related disorder	GLikely benign
Select item 3057141	NM_175940.3(DUOX1):c.2570G>A (p.Arg857His)	DUOX1 (R857H)	Single nucleotide variant (missense variant)	DUOX1-related disorder	GLikely benign
Select item 2629493	NM_175940.3(DUOX1):c.3789C>A (p.Asp1263Glu)	DUOX1 (D1263E)	Single nucleotide variant (missense variant)	DUOX1-related disorder	GUncertain significance

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