ClinVar Miner

Submissions for variant NM_000397.4(CYBB):c.1587-6C>T

gnomAD frequency: 0.00008  dbSNP: rs369705608
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001407409 SCV001609385 likely benign Granulomatous disease, chronic, X-linked 2020-11-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836029 SCV002087155 likely benign Chronic granulomatous disease 2021-07-16 no assertion criteria provided clinical testing

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