ClinVar Miner

Submissions for variant NM_016302.4(CRBN):c.654A>G (p.Gln218=)

gnomAD frequency: 0.00013  dbSNP: rs373145132
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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 RCV000194970 SCV000247094 uncertain significance not specified 2014-07-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000921829 SCV001067242 likely benign not provided 2018-11-13 criteria provided, single submitter clinical testing

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