ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1719G>A (p.Leu573=)

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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 RCV003014973 SCV003318391 likely benign Familial hemiplegic migraine 2022-03-02 criteria provided, single submitter clinical testing

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