ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.89753T>C (p.Val29918Ala)

gnomAD frequency: 0.00003  dbSNP: rs768749427
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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 RCV000852492 SCV000995188 uncertain significance Cardiomyopathy 2019-03-15 criteria provided, single submitter clinical testing

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