ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1224T>C (p.Thr408=)

dbSNP: rs2101989424
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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 RCV002114663 SCV002441153 likely benign Familial hemiplegic migraine 2020-11-10 criteria provided, single submitter clinical testing

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