List of variants in gene DUOX2 reported as pathogenic by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.3328C>T (p.Arg1110Ter)	rs531536885	0.00004
NM_001363711.2(DUOX2):c.2895_2898del (p.Phe966fs)	rs530719719
NM_001363711.2(DUOX2):c.602dup (p.Gln202fs)	rs567500345

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