ClinVar Miner

Submissions for variant NM_000397.3(CYBB):c.1166G>C (p.Gly389Ala) (rs137854586)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000011668 SCV000031900 pathogenic Granulomatous disease, chronic, X-linked, variant 1991-06-01 no assertion criteria provided literature only
UniProtKB/Swiss-Prot RCV000059232 SCV000090761 not provided not provided no assertion provided not provided

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