ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.29564A>G (p.Glu9855Gly)

gnomAD frequency: 0.00001  dbSNP: rs794727011
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000173932 SCV000225112 uncertain significance not provided 2015-03-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000550861 SCV000642949 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-06-05 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000173932 SCV003821202 uncertain significance not provided 2019-10-23 criteria provided, single submitter clinical testing

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