ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.2264G>C (p.Gly755Ala)

dbSNP: rs606231434
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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 RCV001381006 SCV001579255 pathogenic Dystonia 12 2021-08-31 criteria provided, single submitter clinical testing

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