ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.96+8G>T

gnomAD frequency: 0.00006  dbSNP: rs973997819
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001392616 SCV001594261 likely benign Werner syndrome 2024-01-29 criteria provided, single submitter clinical testing

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