ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.70562C>G (p.Thr23521Arg)

gnomAD frequency: 0.00001  dbSNP: rs775589244
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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
GeneDx RCV001565624 SCV001789007 likely benign not provided 2020-02-03 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001565624 SCV003819557 uncertain significance not provided 2019-06-19 criteria provided, single submitter clinical testing

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