ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.3858C>G (p.Thr1286=)

dbSNP: rs558520674
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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 RCV000587612 SCV000694456 likely benign not specified 2019-08-21 criteria provided, single submitter clinical testing
Invitae RCV001419622 SCV001621882 likely benign Wilson disease 2023-06-09 criteria provided, single submitter clinical testing

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