ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.2403_2404del (p.Ile801fs)

dbSNP: rs1765814665
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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 and Genomics, Karolinska University Hospital RCV001269658 SCV001449802 pathogenic not provided 2015-04-27 criteria provided, single submitter clinical testing

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