ClinVar Miner

Submissions for variant NM_019066.5(MAGEL2):c.980C>T (p.Ala327Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV002291484 SCV002583806 uncertain significance not provided 2022-08-01 criteria provided, single submitter clinical testing PM2

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