ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.1981+7G>A

dbSNP: rs2130203751
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
Invitae RCV001456782 SCV001660569 likely benign Werner syndrome 2022-02-03 criteria provided, single submitter clinical testing

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