ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.54653G>A (p.Arg18218Gln)

gnomAD frequency: 0.00001  dbSNP: rs143643360
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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 RCV001288571 SCV001475781 uncertain significance not provided 2020-06-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001288571 SCV003826056 uncertain significance not provided 2021-03-25 criteria provided, single submitter clinical testing

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