ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.13-15_13-12del

dbSNP: rs1184627670
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595587 SCV001829854 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005094845 SCV005812917 likely benign Familial hemiplegic migraine 2024-04-06 criteria provided, single submitter clinical testing

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