List of variants in gene combination CYBB, LOC130068093 reported as likely benign for Granulomatous disease, chronic, X-linked

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000397.4(CYBB):c.43A>G (p.Ile15Val)	rs781809179	0.00001
NM_000397.4(CYBB):c.45+18A>G	rs781908342	0.00001
NM_000397.4(CYBB):c.27G>A (p.Gly9=)
NM_000397.4(CYBB):c.27G>T (p.Gly9=)	rs979166608
NM_000397.4(CYBB):c.30C>A (p.Leu10=)	rs781966553
NM_000397.4(CYBB):c.33C>T (p.Ser11=)
NM_000397.4(CYBB):c.39T>C (p.Phe13=)
NM_000397.4(CYBB):c.42C>A (p.Val14=)	rs1928916724
NM_000397.4(CYBB):c.45+20A>G
NM_000397.4(CYBB):c.45+8C>T
NM_000397.4(CYBB):c.45+9C>G	rs2146802012

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