ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.599_600insACCGGC (p.186_187AP[11])

dbSNP: rs771450542
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000229661 SCV000283425 likely benign Beckwith-Wiedemann syndrome 2024-01-25 criteria provided, single submitter clinical testing
Knight Diagnostic Laboratories, Oregon Health and Sciences University RCV001270080 SCV001448865 benign not provided 2018-09-13 criteria provided, single submitter clinical testing

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