ClinVar Miner

Submissions for variant NM_024344.1:c.2362_2363delinsTCATCT

Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics and Genomics, Karolinska University Hospital RCV001269747 SCV001449982 pathogenic not provided 2020-02-10 criteria provided, single submitter clinical testing

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