ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3318_3319del (p.Asn1106fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV004599134 SCV005092347 pathogenic not provided 2024-10-01 criteria provided, single submitter clinical testing DMD: PVS1, PM2

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