ClinVar Miner

Submissions for variant NM_001939.3(DRP2):c.1845G>A (p.Gln615=)

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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 RCV005184775 SCV005817446 likely benign not provided 2024-09-21 criteria provided, single submitter clinical testing

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