ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.588C>A (p.Arg196=)

gnomAD frequency: 0.00002  dbSNP: rs759197788
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000557118 SCV000629734 likely benign Werner syndrome 2024-03-12 criteria provided, single submitter clinical testing

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