ClinVar Miner

Submissions for variant NM_006593.4(TBR1):c.163dup (p.Ile55fs)

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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 Medical Genetics and Applied Genomics, University Hospital Tübingen RCV004577968 SCV005061856 pathogenic Autism, susceptibility to, 5 2024-06-26 criteria provided, single submitter clinical testing

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