ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.25708G>A (p.Glu8570Lys)

gnomAD frequency: 0.00008  dbSNP: rs552462622
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
Eurofins Ntd Llc (ga) RCV000597777 SCV000701263 uncertain significance not provided 2017-02-17 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000597777 SCV003818426 uncertain significance not provided 2020-06-03 criteria provided, single submitter clinical testing

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