List of variants in gene DUOX2 reported as uncertain significance for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.598G>A (p.Gly200Arg)	rs2467827	0.00146
NM_001363711.2(DUOX2):c.1709A>T (p.Gln570Leu)	rs547116063	0.00131
NM_001363711.2(DUOX2):c.3232G>A (p.Val1078Met)	rs147772932	0.00130
NM_001363711.2(DUOX2):c.1547G>A (p.Arg516His)	rs143818717	0.00029
NM_001363711.2(DUOX2):c.1060C>T (p.Arg354Trp)	rs766496010	0.00014
NM_001363711.2(DUOX2):c.3116G>A (p.Arg1039Gln)	rs772992566	0.00001
NM_001363711.2(DUOX2):c.1587G>T (p.Lys529Asn)
NM_001363711.2(DUOX2):c.1718A>G (p.Gln573Arg)
NM_001363711.2(DUOX2):c.199G>A (p.Asp67Asn)	rs1255757517
NM_001363711.2(DUOX2):c.214G>T (p.Ala72Ser)
NM_001363711.2(DUOX2):c.2793_2796delinsCAAT (p.Asp932Asn)	rs1064796650
NM_001363711.2(DUOX2):c.2803C>T (p.Leu935Phe)
NM_001363711.2(DUOX2):c.3395T>A (p.Met1132Lys)
NM_001363711.2(DUOX2):c.355G>C (p.Val119Leu)	rs138970496
NM_001363711.2(DUOX2):c.3721A>T (p.Ile1241Phe)
NM_001363711.2(DUOX2):c.3830C>G (p.Ala1277Gly)	rs143471358
NM_001363711.2(DUOX2):c.3940G>A (p.Glu1314Lys)
NM_001363711.2(DUOX2):c.587_619del (p.Arg196_Gly206del)	rs1894402738
NM_001363711.2(DUOX2):c.838G>A (p.Glu280Lys)

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