ClinVar Miner

Submissions for variant NM_000053.4(ATP7B):c.3548C>G (p.Ala1183Gly) (rs587783315)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000145277 SCV000192348 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
Counsyl RCV000667056 SCV000791449 uncertain significance Wilson disease 2017-05-16 criteria provided, single submitter clinical testing
Mendelics RCV000667056 SCV001139350 benign Wilson disease 2019-05-28 criteria provided, single submitter clinical testing

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