ClinVar Miner

Submissions for variant NM_000553.5(WRN):c.4015G>A (p.Val1339Ile) (rs11574395)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ITMI RCV000122297 SCV000086524 not provided not specified 2013-09-19 no assertion provided reference population
Invitae RCV000234534 SCV000285573 benign Werner syndrome 2018-01-04 criteria provided, single submitter clinical testing

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