ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.19289A>G (p.Tyr6430Cys)

gnomAD frequency: 0.00002  dbSNP: rs781726929
Minimum review status: Collection method:
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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 RCV000852900 SCV000995637 likely benign Long QT syndrome 2018-05-26 criteria provided, single submitter clinical testing

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