ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.4191G>A (p.Glu1397=) (rs369276959)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ITMI RCV000122299 SCV000086526 not provided not specified 2013-09-19 no assertion provided reference population
Invitae RCV000473088 SCV000541474 likely benign Werner syndrome 2017-12-06 criteria provided, single submitter clinical testing

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