ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.39079A>G (p.Lys13027Glu)

gnomAD frequency: 0.00001  dbSNP: rs761060142
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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 RCV001588099 SCV001823450 uncertain significance not provided 2020-04-30 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001588099 SCV003822989 uncertain significance not provided 2020-05-04 criteria provided, single submitter clinical testing

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