ClinVar Miner

Submissions for variant NM_006721.4(ADK):c.727-8del

dbSNP: rs112610475
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
Mendelics RCV000988387 SCV001138088 benign Adenosine kinase deficiency 2019-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001522753 SCV001732349 benign not provided 2025-01-31 criteria provided, single submitter clinical testing

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