List of variants in gene DUOX2 reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.1921G>A (p.Glu641Lys)	rs139161034	0.00343
NM_001363711.2(DUOX2):c.567C>T (p.His189=)	rs2467829	0.00099
NM_001363711.2(DUOX2):c.2335-3C>T	rs369394906	0.00017
NM_001363711.2(DUOX2):c.3416-13C>T	rs1555412892

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