ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.6461T>C (p.Val2154Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, Skane University Hospital Lund RCV004698036 SCV005198107 uncertain significance not provided 2022-05-27 criteria provided, single submitter clinical testing

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