ClinVar Miner

Submissions for variant NM_000397.3(CYBB):c.1090G>C (p.Gly364Arg) (rs141756032)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000536594 SCV000639752 benign Chronic granulomatous disease, X-linked 2017-10-05 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000595175 SCV000702803 benign not specified 2016-11-10 criteria provided, single submitter clinical testing
UniProtKB/Swiss-Prot RCV000059230 SCV000090759 not provided not provided no assertion provided not provided

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