ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.1851T>C (p.Ile617=)

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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 RCV005142156 SCV005769270 likely benign Dystonia 12 2025-01-30 criteria provided, single submitter clinical testing

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