ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.1466A>G (p.Asn489Ser)

dbSNP: rs2075199183
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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 RCV001316724 SCV001507357 uncertain significance Dystonia 12 2021-09-01 criteria provided, single submitter clinical testing

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