ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3582G>T (p.Thr1194=)

gnomAD frequency: 0.00006  dbSNP: rs762685242
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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 RCV000558067 SCV000629697 likely benign Werner syndrome 2023-11-14 criteria provided, single submitter clinical testing

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