ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.2819+10G>A

gnomAD frequency: 0.00006  dbSNP: rs782236178
Minimum review status: Collection method:
Minimum conflict level:
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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 RCV000870033 SCV001011503 likely benign Dystonia 12 2023-12-27 criteria provided, single submitter clinical testing

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