ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.-10-9C>T

dbSNP: rs878853624
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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 RCV001432695 SCV001635472 likely benign Beckwith-Wiedemann syndrome 2023-01-06 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004597763 SCV005093027 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing CDKN1C: PM2:Supporting, BP4, BP7

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