ClinVar Miner

Submissions for variant NM_006593.4(TBR1):c.691A>G (p.Arg231Gly)

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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 RCV003484544 SCV004229101 likely pathogenic Autism, susceptibility to, 5 2023-10-05 criteria provided, single submitter clinical testing

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