ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.2650G>A (p.Ala884Thr)

gnomAD frequency: 0.00003  dbSNP: rs772195446
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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
Eurofins Ntd Llc (ga) RCV000727450 SCV000708672 uncertain significance not provided 2017-05-24 criteria provided, single submitter clinical testing
GeneDx RCV000727450 SCV000717355 likely benign not provided 2018-11-05 criteria provided, single submitter clinical testing

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