ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.655-20A>G

gnomAD frequency: 0.00001  dbSNP: rs1056118121
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001894074 SCV002122169 likely benign Werner syndrome 2024-05-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001894074 SCV002793516 uncertain significance Werner syndrome 2021-11-12 criteria provided, single submitter clinical testing

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