ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.1692T>C (p.Asp564=)

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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 RCV005165169 SCV005795468 likely benign Dystonia 12 2024-08-01 criteria provided, single submitter clinical testing

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