ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.14296G>A (p.Asp4766Asn)

dbSNP: rs981499527
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000530231 SCV000642689 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-04-17 criteria provided, single submitter clinical testing
AiLife Diagnostics, AiLife Diagnostics RCV002223866 SCV002502594 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing

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