ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.-42_-40GGC[5] (rs71329437)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000356956 SCV000345058 benign not specified 2016-08-17 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000308352 SCV000479324 benign Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000308352 SCV000479328 uncertain significance Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001668623 SCV000730490 benign not provided 2018-06-01 criteria provided, single submitter clinical testing
GeneDx RCV001668623 SCV001891193 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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