ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.10940G>A (p.Ser3647Asn) (rs759642119)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000242239 SCV000318276 uncertain significance Cardiovascular phenotype 2013-02-08 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
CeGaT Praxis fuer Humangenetik Tuebingen RCV000999365 SCV001155942 uncertain significance not provided 2018-08-01 criteria provided, single submitter clinical testing

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