ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.4127C>T (p.Pro1376Leu) (rs146055899)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000547973 SCV000629719 likely benign Werner syndrome 2020-12-01 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000547973 SCV000897451 uncertain significance Werner syndrome 2018-10-31 criteria provided, single submitter clinical testing
ITMI RCV000122296 SCV000086523 not provided not specified 2013-09-19 no assertion provided reference population

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