ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.178-20G>A

gnomAD frequency: 0.00002  dbSNP: rs1306231956
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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 RCV001941972 SCV002235043 likely benign Familial hemiplegic migraine 2024-10-01 criteria provided, single submitter clinical testing

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