ClinVar Miner

Submissions for variant NM_017831.4(RNF125):c.420_423del (p.Cys141fs)

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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 RCV002463396 SCV002757818 uncertain significance Tenorio syndrome 2020-10-30 criteria provided, single submitter clinical testing

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