ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.86445C>G (p.Ala28815=)

dbSNP: rs1459326742
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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 RCV001436481 SCV001639323 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-02-05 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003136076 SCV003819662 uncertain significance not provided 2019-08-22 criteria provided, single submitter clinical testing

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