ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.97493-5T>C

dbSNP: rs886042619
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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) RCV000330621 SCV000335474 uncertain significance not provided 2015-10-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003765603 SCV004588407 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-08-30 criteria provided, single submitter clinical testing

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