ClinVar Miner

Submissions for variant NM_000244.3(MEN1):c.1671T>C (p.Thr557=) (rs143423552)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000490999 SCV000579678 likely benign Hereditary cancer-predisposing syndrome 2014-04-02 criteria provided, single submitter clinical testing
Invitae RCV000123384 SCV000166708 likely benign Multiple endocrine neoplasia, type 1 2017-07-26 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679253 SCV000805924 likely benign not provided 2017-12-05 criteria provided, single submitter clinical testing

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