ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.13-20G>A

gnomAD frequency: 0.00002  dbSNP: rs867285806
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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 RCV002133631 SCV002455507 likely benign Familial hemiplegic migraine 2022-11-22 criteria provided, single submitter clinical testing

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