ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.876A>C (p.Leu292=)

dbSNP: rs759323644
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002186454 SCV002483756 likely benign Werner syndrome 2020-12-27 criteria provided, single submitter clinical testing

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