ClinVar Miner

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

dbSNP: rs34423002
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719375 SCV001948174 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827590 SCV002082966 benign Pontocerebellar hypoplasia type 2D 2019-09-27 no assertion criteria provided clinical testing

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