ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3459+6G>C

gnomAD frequency: 0.00001  dbSNP: rs781501590
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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 RCV000230150 SCV000285563 likely benign Werner syndrome 2024-02-22 criteria provided, single submitter clinical testing

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