ClinVar Miner

Submissions for variant NM_001206999.2(CIT):c.5623+9G>A

gnomAD frequency: 0.00708  dbSNP: rs11610278
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 RCV000954737 SCV001101390 benign not provided 2025-01-14 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818994 SCV002064938 benign not specified 2017-09-28 criteria provided, single submitter clinical testing

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