ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.900G>A (p.Pro300=)

dbSNP: rs1364915876
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000876278 SCV001018834 likely benign Beckwith-Wiedemann syndrome 2023-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705851 SCV005223194 likely benign not provided criteria provided, single submitter not provided

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