ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2157C>T (p.Ser719=)

dbSNP: rs2101995092
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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 RCV001474959 SCV001679137 likely benign Familial hemiplegic migraine 2022-02-24 criteria provided, single submitter clinical testing

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