ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.407C>T (p.Ala136Val)

dbSNP: rs1651502620
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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 RCV001314710 SCV001505254 uncertain significance Familial hemiplegic migraine 2021-08-26 criteria provided, single submitter clinical testing

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