ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1462-17A>G

dbSNP: rs1570989962
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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 RCV002202693 SCV002356784 likely benign Familial hemiplegic migraine 2023-05-07 criteria provided, single submitter clinical testing

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