ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.103524C>G (p.Val34508=)

dbSNP: rs587780985
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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) RCV000734757 SCV000862925 uncertain significance not provided 2018-08-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001437533 SCV001640387 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-03-09 criteria provided, single submitter clinical testing

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