ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.104179A>G (p.Arg34727Gly)

gnomAD frequency: 0.00003  dbSNP: rs555555534
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704937 SCV000237922 likely benign not provided 2020-02-04 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001704937 SCV003819591 uncertain significance not provided 2019-11-25 criteria provided, single submitter clinical testing

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