ClinVar Miner

Submissions for variant NM_001332.4(CTNND2):c.2277+1del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV005002113 SCV005627690 uncertain significance Complex neurodevelopmental disorder 2024-10-29 criteria provided, single submitter clinical testing

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