ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1827+10del

dbSNP: rs1651741885
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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 RCV001473063 SCV001677207 likely benign Familial hemiplegic migraine 2022-10-14 criteria provided, single submitter clinical testing

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