ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.*5+1G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003333611 SCV004041362 uncertain significance IMAGe syndrome 2023-02-27 criteria provided, single submitter clinical testing
Baylor Genetics RCV003333610 SCV004041423 uncertain significance Beckwith-Wiedemann syndrome 2023-02-27 criteria provided, single submitter clinical testing

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