ClinVar Miner

Submissions for variant NM_000702.4(ATP1A2):c.2450T>A (p.Ile817Asn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004515793 SCV005016580 uncertain significance Migraine, familial hemiplegic, 2 2024-03-14 criteria provided, single submitter clinical testing

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