ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.62del (p.Lys21fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004012648 SCV004841353 likely pathogenic Wilson disease 2023-12-01 criteria provided, single submitter clinical testing

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