ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.95A>G (p.Lys32Arg) (rs34477820)

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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 RCV000122279 SCV000227158 benign not specified 2015-04-24 criteria provided, single submitter clinical testing
ITMI RCV000122279 SCV000086504 not provided not specified 2013-09-19 no assertion provided reference population
Illumina Clinical Services Laboratory,Illumina RCV000344080 SCV000473309 uncertain significance Werner syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000344080 SCV000554390 benign Werner syndrome 2018-01-03 criteria provided, single submitter clinical testing

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