ClinVar Miner

Submissions for variant NM_152296.5(ATP1A3):c.6+7G>A

dbSNP: rs2145995390
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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 RCV001449008 SCV001652112 likely benign Dystonia 12 2019-12-11 criteria provided, single submitter clinical testing

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