ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76994T>G (p.Leu25665Arg)

gnomAD frequency: 0.00001  dbSNP: rs188012906
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001289393 SCV001477168 uncertain significance not provided 2020-06-03 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001289393 SCV003819604 uncertain significance not provided 2019-08-29 criteria provided, single submitter clinical testing

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