List of variants in gene DUOX2 reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001363711.2(DUOX2):c.3006-2A>G	rs371960046	0.00012
NM_001363711.2(DUOX2):c.2335-1G>C	rs758001307	0.00001
NM_001363711.2(DUOX2):c.345_352del (p.Asp115fs)	rs1566978577
NM_001363711.2(DUOX2):c.4524+1G>C
NM_001363711.2(DUOX2):c.4537G>C (p.Gly1513Arg)
NM_001363711.2(DUOX2):c.534G>T (p.Trp178Cys)
NM_001363711.2(DUOX2):c.857G>A (p.Arg286His)

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