ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.885G>C (p.Gly295=)

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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 RCV002676894 SCV002990807 likely benign Familial hemiplegic migraine 2024-05-15 criteria provided, single submitter clinical testing

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