ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.65790C>A (p.Asp21930Glu)

gnomAD frequency: 0.00001  dbSNP: rs794727432
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) RCV000176703 SCV000228403 uncertain significance not provided 2015-03-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000176703 SCV003821201 uncertain significance not provided 2019-10-23 criteria provided, single submitter clinical testing

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