ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.1285+8G>C

dbSNP: rs377584333
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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 RCV001425927 SCV001628565 likely benign Wilson disease 2021-04-06 criteria provided, single submitter clinical testing

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