ClinVar Miner

Submissions for variant NM_000397.4(CYBB):c.328C>T (p.Leu110Phe)

dbSNP: rs1929209834
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
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004526833 SCV005039120 uncertain significance not specified 2024-03-25 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279971 SCV001467110 uncertain significance Chronic granulomatous disease 2020-08-13 no assertion criteria provided clinical testing

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