ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.1806+12G>A

gnomAD frequency: 0.00001  dbSNP: rs1555862070
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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 RCV002100432 SCV002383596 likely benign Dystonia 12 2023-08-04 criteria provided, single submitter clinical testing

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