ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3222G>C (p.Leu1074Phe)

dbSNP: rs1801195
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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 RCV001434072 SCV001636873 likely benign Werner syndrome 2023-06-02 criteria provided, single submitter clinical testing

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