ClinVar Miner

Submissions for variant NM_016302.4(CRBN):c.175-5T>A

gnomAD frequency: 0.01132  dbSNP: rs151039737
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
Genetic Services Laboratory, University of Chicago RCV000116834 SCV000150908 likely benign not specified 2013-05-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707957 SCV005245058 benign not provided criteria provided, single submitter not provided

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