ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.29305T>C (p.Tyr9769His)

gnomAD frequency: 0.00001  dbSNP: rs778087108
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego RCV000852881 SCV000995615 likely benign Cardiomyopathy 2019-06-03 criteria provided, single submitter clinical testing

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