ClinVar Miner

Submissions for variant NM_001012339.3(DNAJC21):c.279C>T (p.Thr93=)

gnomAD frequency: 0.00002  dbSNP: rs541503410
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000942299 SCV001088221 likely benign not provided 2024-12-17 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818915 SCV002065536 uncertain significance not specified 2017-11-21 criteria provided, single submitter clinical testing

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