ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.95185T>C (p.Trp31729Arg)

dbSNP: rs869320741
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986937 SCV001136096 pathogenic Dilated cardiomyopathy 1G 2019-05-28 criteria provided, single submitter clinical testing
GeneReviews RCV000119022 SCV000153724 pathogenic Myopathy, myofibrillar, 9, with early respiratory failure 2014-02-27 no assertion criteria provided literature only

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