ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.561T>C (p.Tyr187=)

dbSNP: rs1162659137
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002069608 SCV002343416 likely benign Wilson disease 2022-04-30 criteria provided, single submitter clinical testing

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