ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.66174C>T (p.Arg22058=)

dbSNP: rs886043463
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000274801 SCV000340273 uncertain significance not provided 2016-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005222871 SCV005868035 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-04-16 criteria provided, single submitter clinical testing

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