ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.1174-4T>G

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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 Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn RCV004776551 SCV005387926 uncertain significance Chromosome 2q32-q33 deletion syndrome 2024-09-12 criteria provided, single submitter clinical testing

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