ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.59888T>C (p.Val19963Ala)

dbSNP: rs1553645836
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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 RCV000643251 SCV000764938 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-12-27 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000728966 SCV000856595 uncertain significance not provided 2017-08-25 criteria provided, single submitter clinical testing

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