ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1652-8C>A

dbSNP: rs370023134
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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 RCV002192918 SCV002354439 likely benign Familial hemiplegic migraine 2023-11-27 criteria provided, single submitter clinical testing

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