ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.1734T>C (p.Ser578=)

dbSNP: rs867210698
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 RCV001467924 SCV001671956 likely benign Werner syndrome 2025-01-23 criteria provided, single submitter clinical testing

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