ClinVar Miner

Submissions for variant NM_001079872.2(CUL4B):c.1257-19T>C

gnomAD frequency: 0.00205  dbSNP: rs201629851
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 RCV002113535 SCV002402268 benign X-linked intellectual disability Cabezas type 2024-12-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714368 SCV005277997 benign not provided criteria provided, single submitter not provided

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