ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.963C>T (p.Phe321=)

dbSNP: rs1651629750
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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 RCV001431122 SCV001633874 likely benign Familial hemiplegic migraine 2019-05-04 criteria provided, single submitter clinical testing

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