ClinVar Miner

Submissions for variant NM_000096.4(CP):c.1100G>A (p.Arg367His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV004792153 SCV005410438 uncertain significance not provided 2024-08-20 criteria provided, single submitter clinical testing PM2
Labcorp Genetics (formerly Invitae), Labcorp RCV005105089 SCV005816292 likely benign Deficiency of ferroxidase 2024-02-28 criteria provided, single submitter clinical testing

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