ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1017+7G>A

gnomAD frequency: 0.00001  dbSNP: rs1438633873
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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 RCV000791477 SCV000930728 likely benign Familial hemiplegic migraine 2024-02-17 criteria provided, single submitter clinical testing

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