ClinVar Miner

Submissions for variant NM_130797.4(DPP6):c.1388T>C (p.Ile463Thr)

dbSNP: rs1554471895
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000626220 SCV000746865 uncertain significance Intellectual disability, autosomal dominant 33 2017-12-18 criteria provided, single submitter clinical testing

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