ClinVar Miner

Submissions for variant NM_001195553.2(DCX):c.339C>A (p.Ile113=)

gnomAD frequency: 0.00001  dbSNP: rs587783543
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000145837 SCV000192974 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001311096 SCV001501139 likely benign not provided 2020-12-01 criteria provided, single submitter clinical testing
Invitae RCV001311096 SCV002994016 benign not provided 2022-07-06 criteria provided, single submitter clinical testing

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