ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.4035G>A (p.Thr1345=)

gnomAD frequency: 0.00001  dbSNP: rs767115441
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000276259 SCV000345291 uncertain significance not provided 2016-09-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001087786 SCV000629716 likely benign Werner syndrome 2024-10-24 criteria provided, single submitter clinical testing

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