ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.-19_-18insGGCACCGGC

dbSNP: rs1554617688
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000273136 SCV000479330 uncertain significance Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001675886 SCV001892940 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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