ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.107182G>A (p.Glu35728Lys)

gnomAD frequency: 0.00001  dbSNP: rs764891218
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000404735 SCV000344910 uncertain significance not provided 2016-09-03 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000404735 SCV002770630 uncertain significance not provided 2022-07-26 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000404735 SCV003819693 uncertain significance not provided 2022-05-11 criteria provided, single submitter clinical testing

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