ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.13115del (p.Val4372fs)

dbSNP: rs2154317965
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centogene AG - the Rare Disease Company RCV001809050 SCV002059400 likely pathogenic Dilated cardiomyopathy 1G 2019-06-05 criteria provided, single submitter clinical testing
Center for Human Genetics, University of Leuven RCV003237360 SCV002817399 likely pathogenic Primary dilated cardiomyopathy 2022-12-31 criteria provided, single submitter clinical testing

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