ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3525A>G (p.Pro1175=)

dbSNP: rs2130440993
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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 RCV002138298 SCV002459835 likely benign Werner syndrome 2023-07-31 criteria provided, single submitter clinical testing

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