ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.724+14C>T

dbSNP: rs1455016344
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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 RCV002071237 SCV002326085 likely benign Werner syndrome 2023-06-12 criteria provided, single submitter clinical testing

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