ClinVar Miner

Submissions for variant NC_000004.11:g.148550590_148578202dup

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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
Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University RCV003126226 SCV002569986 uncertain significance Neurodevelopmental abnormality 2022-08-02 criteria provided, single submitter research

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