ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.14878T>C (p.Cys4960Arg)

dbSNP: rs879004875
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
AiLife Diagnostics, AiLife Diagnostics RCV002223474 SCV002501078 uncertain significance not provided 2022-01-07 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002282699 SCV002571827 uncertain significance not specified 2022-08-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002223474 SCV005188159 uncertain significance not provided criteria provided, single submitter not provided

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