ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3309+13G>T

gnomAD frequency: 0.00004  dbSNP: rs554036292
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 RCV002159923 SCV002413796 benign Werner syndrome 2024-11-05 criteria provided, single submitter clinical testing

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