ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.80167C>T (p.Arg26723Cys)

gnomAD frequency: 0.00001  dbSNP: rs1412497882
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003143239 SCV003824248 uncertain significance not provided 2023-09-15 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV005405992 SCV006065087 likely benign not specified 2025-04-09 criteria provided, single submitter clinical testing

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