ClinVar Miner

Submissions for variant NM_015141.4(GPD1L):c.111A>G (p.Thr37=)

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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 RCV005148817 SCV005776093 likely benign Brugada syndrome 2024-06-02 criteria provided, single submitter clinical testing

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