ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.-42_-40GGC[9] (rs71329437)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000289387 SCV000341736 likely benign not specified 2016-05-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000338938 SCV000479323 uncertain significance Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000338938 SCV000479326 benign Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
Genetic Services Laboratory,University of Chicago RCV000289387 SCV000597847 uncertain significance not specified 2016-05-19 criteria provided, single submitter clinical testing

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