ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.106160C>G (p.Ser35387Ter)

dbSNP: rs2154132755
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001785099 SCV002022472 pathogenic not provided 2022-06-09 criteria provided, single submitter clinical testing
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004527432 SCV005038827 pathogenic Dilated cardiomyopathy 1G 2024-03-14 criteria provided, single submitter clinical testing

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