List of variants in gene DUOX2 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.3515+15T>A	rs269869	0.99253
NM_001363711.2(DUOX2):c.413C>T (p.Pro138Leu)	rs2001616	0.75375
NM_001363711.2(DUOX2):c.3200C>T (p.Ser1067Leu)	rs269868	0.71631
NM_001363711.2(DUOX2):c.2033A>G (p.His678Arg)	rs57659670	0.17189
NM_001363711.2(DUOX2):c.2334+10C>T	rs73406330	0.09464
NM_001363711.2(DUOX2):c.4479C>G (p.Pro1493=)	rs56323146	0.08342
NM_001363711.2(DUOX2):c.2286G>A (p.Gln762=)	rs73406334	0.07585
NM_001363711.2(DUOX2):c.2148+9C>T	rs73406337	0.07581
NM_001363711.2(DUOX2):c.2102G>A (p.Arg701Gln)	rs113400262	0.04972
NM_001363711.2(DUOX2):c.3966C>T (p.Ser1322=)	rs61730032	0.02613
NM_001363711.2(DUOX2):c.1693+10G>A	rs76411432	0.02317
NM_001363711.2(DUOX2):c.3261G>A (p.Ala1087=)	rs79480907	0.01330
NM_001363711.2(DUOX2):c.908C>G (p.Pro303Arg)	rs151261408	0.01090
NM_001363711.2(DUOX2):c.2182G>A (p.Ala728Thr)	rs138353181	0.00700
NM_001363711.2(DUOX2):c.3856T>C (p.Tyr1286His)	rs148968706	0.00452
NM_001363711.2(DUOX2):c.3081G>A (p.Lys1027=)	rs78876145	0.00338
NM_001363711.2(DUOX2):c.3759G>A (p.Pro1253=)	rs140663764	0.00307
NM_001363711.2(DUOX2):c.1621C>A (p.Arg541=)	rs140940946	0.00096
NM_001363711.2(DUOX2):c.3055A>G (p.Met1019Val)	rs148053632	0.00086
NM_001363711.2(DUOX2):c.243G>A (p.Pro81=)	rs369158930	0.00056
NM_001363711.2(DUOX2):c.1461G>C (p.Gly487=)	rs269860
NM_001363711.2(DUOX2):c.2944C>G (p.Pro982Ala)	rs61730030

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