ClinVar Miner

Submissions for variant NM_001007027.2(ALG8):c.*272A>G (rs1263505)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000606377 SCV000733112 benign Congenital disorder of glycosylation type 1H no assertion criteria provided clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000082154 SCV000114100 benign not specified 2012-07-25 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000377689 SCV000374557 benign Congenital disorder of glycosylation 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000082154 SCV000314243 benign not specified criteria provided, single submitter clinical testing

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