ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.2325C>A (p.Ala775=)

dbSNP: rs755218710
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000922628 SCV001068065 likely benign Wilson disease 2023-03-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000922628 SCV004833910 likely benign Wilson disease 2023-08-15 criteria provided, single submitter clinical testing

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