ClinVar Miner

Submissions for variant NM_207037.2(TCF12):c.268C>T (p.Arg90Ter)

dbSNP: rs747222651
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Provincial Medical Genetics Program of British Columbia, University of British Columbia RCV002071018 SCV002320802 likely pathogenic TCF12-related craniosynostosis 2022-01-01 criteria provided, single submitter clinical testing

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