ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.1465T>C (p.Ser489Pro)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003990423 SCV004807046 uncertain significance Migraine, familial hemiplegic, 2 2024-03-26 criteria provided, single submitter clinical testing

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