ClinVar Miner

Submissions for variant NM_130797.4(DPP6):c.226G>A (p.Asp76Asn)

gnomAD frequency: 0.02864  dbSNP: rs569787719
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000425085 SCV000511337 likely benign not provided 2016-06-10 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
Clinical Genetics, Academic Medical Center RCV000425085 SCV001923803 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727713 SCV001974956 benign not specified no assertion criteria provided clinical testing

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