List of variants in gene combination CYBB, LOC130068093 reported as uncertain significance for hematologic disorder

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_000397.4(CYBB):c.32C>T (p.Ser11Phe)
NM_000397.4(CYBB):c.43A>T (p.Ile15Phe)	rs781809179
NM_000397.4(CYBB):c.45+3A>C	rs1602173466

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