List of variants in gene CYBB reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000397.4(CYBB):c.338-13C>T	rs193922447	0.00064
NM_000397.4(CYBB):c.1496A>C (p.Lys499Thr)	rs201356986	0.00007
NM_000397.4(CYBB):c.1151+13T>C	rs781868409	0.00003
NC_000023.10:g.(?_37639269)_(37672715_?)dup
NM_000397.4(CYBB):c.1165G>A (p.Gly389Arg)	rs1556471150
NM_000397.4(CYBB):c.1565C>T (p.Thr522Ile)
NM_000397.4(CYBB):c.1601T>A (p.Val534Asp)	rs151344478
NM_000397.4(CYBB):c.674+34T>G	rs1569479417
NM_000397.4(CYBB):c.674+62dup	rs1569479419

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