ClinVar Miner

Submissions for variant NM_016955.4(SEPSECS):c.115-18dup

dbSNP: rs34423002
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193641 SCV000248846 benign not specified 2014-11-04 criteria provided, single submitter clinical testing
GeneDx RCV001636717 SCV001849107 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000193641 SCV001920894 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000193641 SCV001967865 benign not specified no assertion criteria provided clinical testing
Natera, Inc. RCV001833140 SCV002082967 benign Pontocerebellar hypoplasia type 2D 2019-09-27 no assertion criteria provided clinical testing

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