ClinVar Miner

Submissions for variant NC_000023.10:g.102632399_103221016del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV001172265 SCV001193437 pathogenic Global developmental delay 2019-12-02 no assertion criteria provided clinical testing

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