List of variants in gene combination CYBB, LOC130068093 reported as likely benign for Chronic granulomatous disease

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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.30C>T (p.Leu10=)	rs781966553	0.00001
NM_000397.4(CYBB):c.43A>G (p.Ile15Val)	rs781809179	0.00001
NM_000397.4(CYBB):c.27G>T (p.Gly9=)	rs979166608

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