ClinVar Miner

Submissions for variant GRCh37/hg19 2q23.1(chr2:149220152-149633312)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Medical Genetics, National & Kapodistrian University of Athens RCV003236740 SCV003935239 likely pathogenic Intellectual disability, autosomal dominant 1 2023-05-26 criteria provided, single submitter clinical testing

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