ClinVar Miner

Submissions for variant NM_014008.5(CCDC22):c.901T>C (p.Phe301Leu)

gnomAD frequency: 0.00048  dbSNP: rs147674513
Minimum review status: Collection method:
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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 RCV000502049 SCV000593900 uncertain significance not specified 2015-09-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000927975 SCV001073576 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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