ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1335A>G (p.Thr445=)

dbSNP: rs1570989335
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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 RCV000983750 SCV001131776 likely benign Familial hemiplegic migraine 2022-10-24 criteria provided, single submitter clinical testing

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