ClinVar Miner

Submissions for variant NM_130797.4(DPP6):c.227A>T (p.Asp76Val)

gnomAD frequency: 0.01073  dbSNP: rs572667303
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia RCV000238936 SCV000297368 likely benign not specified 2015-09-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000513626 SCV000609284 uncertain significance not provided 2017-02-01 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513626 SCV000610995 benign not provided 2017-05-15 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000513626 SCV001923541 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000238936 SCV001951535 benign not specified no assertion criteria provided clinical testing

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