ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.1377C>T (p.Asn459=)

gnomAD frequency: 0.00001  dbSNP: rs746238163
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001422863 SCV001625422 likely benign Werner syndrome 2024-10-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707593 SCV005223354 likely benign not provided criteria provided, single submitter not provided

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