ClinVar Miner

Submissions for variant NM_014974.3(DIP2C):c.262C>T (p.Arg88Trp)

dbSNP: rs965093390
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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 Leipzig Medical Center RCV001253273 SCV001428909 uncertain significance Obesity; Neurodevelopmental delay 2018-01-11 criteria provided, single submitter clinical testing

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