ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.891C>T (p.Phe297=)

gnomAD frequency: 0.00001  dbSNP: rs921400561
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000546242 SCV000645419 likely benign Dystonia 12 2023-10-28 criteria provided, single submitter clinical testing

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