ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2880G>T (p.Ala960=)

dbSNP: rs762969049
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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 RCV000457521 SCV000556860 likely benign Familial hemiplegic migraine 2024-06-26 criteria provided, single submitter clinical testing

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