ClinVar Miner

Submissions for variant NM_014008.5(CCDC22):c.962G>A (p.Arg321Gln)

gnomAD frequency: 0.00054  dbSNP: rs140735182
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000180311 SCV000232721 likely benign not specified 2015-03-12 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000180311 SCV000246910 uncertain significance not specified 2014-12-16 criteria provided, single submitter clinical testing

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