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

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: 52

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HGVS	dbSNP	gnomAD frequency
NM_000397.4(CYBB):c.804+118A>G	rs5964125	0.16667
NM_000397.4(CYBB):c.483+78C>T	rs6610669	0.16506
NM_000397.4(CYBB):c.1002G>A (p.Lys334=)	rs2228117	0.05579
NM_000397.4(CYBB):c.1090G>C (p.Gly364Arg)	rs141756032	0.00371
NM_000397.4(CYBB):c.654C>A (p.Gly218=)	rs35080474	0.00303
NM_000397.4(CYBB):c.1551T>A (p.Asp517Glu)	rs151344452	0.00144
NM_000397.4(CYBB):c.686G>A (p.Arg229His)	rs139670417	0.00106
NM_000397.4(CYBB):c.46-7T>C	rs182039020	0.00070
NM_000397.4(CYBB):c.338-13C>T	rs193922447	0.00064
NM_000397.4(CYBB):c.1159G>A (p.Val387Ile)	rs145620748	0.00043
NM_000397.4(CYBB):c.6G>C (p.Gly2=)	rs372462475	0.00029
NM_000397.4(CYBB):c.805-17T>A	rs182092761	0.00026
NM_000397.4(CYBB):c.1689C>T (p.Phe563=)	rs567830215	0.00023
NM_000397.4(CYBB):c.1414G>A (p.Gly472Ser)	rs13306300	0.00018
NM_000397.4(CYBB):c.855G>A (p.Leu285=)	rs782293433	0.00018
NM_000397.4(CYBB):c.1685A>G (p.His562Arg)	rs768055122	0.00013
NM_000397.4(CYBB):c.675-4C>T	rs782223666	0.00013
NM_000397.4(CYBB):c.142-12C>T	rs13306298	0.00009
NM_000397.4(CYBB):c.1158G>A (p.Ala386=)	rs374511592	0.00007
NM_000397.4(CYBB):c.99T>C (p.Tyr33=)	rs781937944	0.00007
NM_000397.4(CYBB):c.1203T>C (p.Tyr401=)	rs782312337	0.00006
NM_000397.4(CYBB):c.1103C>T (p.Ala368Val)	rs781935760	0.00005
NM_000397.4(CYBB):c.1701G>A (p.Lys567=)	rs140774378	0.00005
NM_000397.4(CYBB):c.697G>A (p.Ala233Thr)	rs374931542	0.00005
NM_000397.4(CYBB):c.1377A>G (p.Gln459=)	rs782413959	0.00004
NM_000397.4(CYBB):c.1413C>T (p.Ala471=)	rs782094378	0.00004
NM_000397.4(CYBB):c.171A>G (p.Ala57=)	rs781824754	0.00004
NM_000397.4(CYBB):c.348C>T (p.Thr116=)	rs782735382	0.00004
NM_000397.4(CYBB):c.1151+13T>C	rs781868409	0.00003
NM_000397.4(CYBB):c.142-6T>C	rs373947610	0.00003
NM_000397.4(CYBB):c.1300C>T (p.Leu434=)	rs781891223	0.00002
NM_000397.4(CYBB):c.10T>A (p.Trp4Arg)	rs782495755	0.00001
NM_000397.4(CYBB):c.1617T>C (p.Pro539=)	rs187038548	0.00001
NM_000397.4(CYBB):c.549G>A (p.Thr183=)	rs1556468340	0.00001
NM_000397.4(CYBB):c.663C>A (p.Ile221=)	rs782727740	0.00001
NM_000397.4(CYBB):c.696C>T (p.Thr232=)	rs782180981	0.00001
NM_000397.4(CYBB):c.1032C>G (p.Ser344=)	rs782193225
NM_000397.4(CYBB):c.1071C>T (p.Ile357=)
NM_000397.4(CYBB):c.1090G>A (p.Gly364Arg)	rs141756032
NM_000397.4(CYBB):c.1151+15C>A
NM_000397.4(CYBB):c.1152-16C>T
NM_000397.4(CYBB):c.1296C>T (p.Thr432=)	rs782808570
NM_000397.4(CYBB):c.1314+16T>C
NM_000397.4(CYBB):c.1314+19C>T	rs34834015
NM_000397.4(CYBB):c.1314+20G>A	rs34290745
NM_000397.4(CYBB):c.1315-9del
NM_000397.4(CYBB):c.1497A>C (p.Lys499Asn)	rs782201696
NM_000397.4(CYBB):c.1681G>A (p.Val561Met)	rs766756667
NM_000397.4(CYBB):c.216T>C (p.Cys72=)	rs782202693
NM_000397.4(CYBB):c.483+13T>A
NM_000397.4(CYBB):c.520T>C (p.Leu174=)
NM_000397.4(CYBB):c.60G>A (p.Gly20=)

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