ClinVar Miner

Submissions for variant NM_000397.4(CYBB):c.1090G>A (p.Gly364Arg)

dbSNP: rs141756032
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083247 SCV002376054 benign Granulomatous disease, chronic, X-linked 2021-07-02 criteria provided, single submitter clinical testing

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