ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.618C>T (p.Asp206=)

dbSNP: rs751669088
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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 RCV001395484 SCV001597197 likely benign Beckwith-Wiedemann syndrome 2019-05-03 criteria provided, single submitter clinical testing

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