ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.855A>G (p.Leu285=)

gnomAD frequency: 0.00001  dbSNP: rs762404436
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001414338 SCV001616471 likely benign Werner syndrome 2025-01-15 criteria provided, single submitter clinical testing

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