ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.788-4G>T

gnomAD frequency: 0.00007  dbSNP: rs764972822
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002155889 SCV002466100 likely benign Beckwith-Wiedemann syndrome 2021-07-20 criteria provided, single submitter clinical testing

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