ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18542G>A (p.Arg6181Gln)

gnomAD frequency: 0.00002  dbSNP: rs201951252
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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 RCV001091084 SCV001779910 likely benign not provided 2020-04-14 criteria provided, single submitter clinical testing
Revvity Omics, Revvity Omics RCV001091084 SCV003819828 uncertain significance not provided 2023-01-11 criteria provided, single submitter clinical testing

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