ClinVar Miner

Submissions for variant NM_004982.4(KCNJ8):c.1104C>T (p.Thr368=)

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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 RCV003540060 SCV004282641 likely benign Brugada syndrome 2023-05-22 criteria provided, single submitter clinical testing

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