ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.26144G>T (p.Cys8715Phe)

dbSNP: rs183499397
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000642941 SCV000764628 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-12-21 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000733717 SCV000861811 uncertain significance not provided 2018-06-13 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000733717 SCV003826631 uncertain significance not provided 2022-09-08 criteria provided, single submitter clinical testing

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