ClinVar Miner

Submissions for variant NM_001079872.2(CUL4B):c.1257-9dup

dbSNP: rs746854249
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000174083 SCV000225321 benign not specified 2014-10-22 criteria provided, single submitter clinical testing
GeneDx RCV001577597 SCV001805000 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002516613 SCV002991746 benign X-linked intellectual disability Cabezas type 2022-02-21 criteria provided, single submitter clinical testing

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