ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.81844A>G (p.Lys27282Glu)

gnomAD frequency: 0.00003  dbSNP: rs761201021
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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 RCV001577886 SCV001805364 likely benign not provided 2020-07-30 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001577886 SCV004237002 uncertain significance not provided 2023-03-28 criteria provided, single submitter clinical testing

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