ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.5308A>G (p.Arg1770Gly)

gnomAD frequency: 0.00003  dbSNP: rs780733773
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001572117 SCV001796701 likely benign not provided 2021-01-21 criteria provided, single submitter clinical testing
KardioGenetik, Herz- und Diabeteszentrum NRW RCV003514509 SCV004363570 uncertain significance Dilated cardiomyopathy 1G 2024-01-29 criteria provided, single submitter clinical testing

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