ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1032G>A (p.Leu344=)

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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 RCV003043961 SCV003338556 likely benign Familial hemiplegic migraine 2024-01-02 criteria provided, single submitter clinical testing

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