ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.2983G>A (p.Ala995Thr) (rs140768346)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000227936 SCV000285548 benign Werner syndrome 2018-01-10 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000122285 SCV000342314 likely benign not specified 2016-05-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000227936 SCV000473340 uncertain significance Werner syndrome 2016-06-14 criteria provided, single submitter clinical testing
ITMI RCV000122285 SCV000086510 not provided not specified 2013-09-19 no assertion provided reference population

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