ClinVar Miner

Submissions for variant NM_130797.4(DPP6):c.2183dup (p.Asn728fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV004595748 SCV005088411 uncertain significance Intellectual disability, autosomal dominant 33 no assertion criteria provided clinical testing

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