List of variants in gene CYBB studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
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.46-7T>C	rs182039020	0.00070
NM_000397.4(CYBB):c.1414G>A (p.Gly472Ser)	rs13306300	0.00018
NM_000397.4(CYBB):c.483+978G>A	rs1031189017	0.00015
NM_000397.4(CYBB):c.1496A>C (p.Lys499Thr)	rs201356986	0.00007
NM_000397.4(CYBB):c.621C>T (p.Tyr207=)	rs371655268	0.00002
NM_000397.4(CYBB):c.1151+19T>G	rs782111012	0.00001
NC_000023.10:g.(?_37639269)_(37672715_?)dup
NM_000397.4(CYBB):c.1314+19C>T	rs34834015
NM_000397.4(CYBB):c.1565C>T (p.Thr522Ile)
NM_000397.4(CYBB):c.1586+74_1586+76dup
NM_000397.4(CYBB):c.674+34T>G	rs1569479417
NM_000397.4(CYBB):c.674+62dup	rs1569479419
NM_000397.4(CYBB):c.860G>A (p.Arg287Gln)

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