ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.86168del (p.Phe28723fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV003493990 SCV004244370 pathogenic Dilated cardiomyopathy 1G 2024-01-19 criteria provided, single submitter clinical testing Criteria applied: PVS1,PS4_SUP,PM2_SUP
Research Unit of Cardiovascular and Metabolic Disease, Inserm RCV003233300 SCV003932078 likely pathogenic Primary dilated cardiomyopathy 2022-07-21 no assertion criteria provided research

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