ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3929A>T (p.Gln1310Leu) (rs2074435)

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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000079454 SCV000111333 benign not specified 2013-11-12 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000079454 SCV000195460 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000079454 SCV000306516 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000403416 SCV000411670 benign Primary Microcephaly 2 With or Without Cortical Malformations 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000710286 SCV000677570 benign not provided 2017-06-05 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000576369 SCV000745383 benign Primary autosomal recessive microcephaly 2 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000576369 SCV000733883 benign Primary autosomal recessive microcephaly 2 no assertion criteria provided clinical testing

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