ClinVar Miner

Submissions for variant NM_181552.4(CUX1):c.2063-8C>T

gnomAD frequency: 0.00222  dbSNP: rs201396561
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000890565 SCV001034320 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000890565 SCV001962071 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing CUX1: BP4, BS1

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