ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.74468C>G (p.Ala24823Gly)

dbSNP: rs368071644
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomics Program, Sidra Medicine RCV001293175 SCV001434173 likely benign Primary dilated cardiomyopathy criteria provided, single submitter research
Revvity Omics, Revvity RCV003135894 SCV003824752 uncertain significance not provided 2022-08-30 criteria provided, single submitter clinical testing

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