ClinVar Miner

Submissions for variant NC_000003.11:g.9387774_9503839del116066

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Cytogenetics and Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano RCV002227505 SCV001167679 pathogenic 3p- syndrome 2020-03-02 criteria provided, single submitter research

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