ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.915C>T (p.Phe305=)

gnomAD frequency: 0.00004  dbSNP: rs376035600
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000761684 SCV000891860 likely benign not provided 2018-07-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067201 SCV002354318 likely benign Familial hemiplegic migraine 2024-03-22 criteria provided, single submitter clinical testing

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