ClinVar Miner

Submissions for variant NM_000553.4(WRN):c.1717A>G (p.Thr573Ala) (rs150148567)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000227669 SCV000473325 uncertain significance Werner syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000227669 SCV000285525 likely benign Werner syndrome 2018-01-10 criteria provided, single submitter clinical testing

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