ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.39344T>C (p.Val13115Ala)

gnomAD frequency: 0.00001  dbSNP: rs762713897
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
Athena Diagnostics RCV000516635 SCV000616069 uncertain significance not specified 2016-11-11 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000731699 SCV000859547 uncertain significance not provided 2018-02-12 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000731699 SCV003826754 uncertain significance not provided 2019-03-12 criteria provided, single submitter clinical testing

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