ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.22576G>T (p.Val7526Phe)

gnomAD frequency: 0.00006  dbSNP: rs754972548
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV001507604 SCV001713246 uncertain significance not provided 2020-11-02 criteria provided, single submitter clinical testing
GeneDx RCV001507604 SCV001786327 likely benign not provided 2019-05-22 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001507604 SCV003826535 uncertain significance not provided 2020-03-18 criteria provided, single submitter clinical testing

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