ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.91998C>G (p.Ala30666=)

dbSNP: rs1160773007
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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) RCV000597857 SCV000704715 uncertain significance not provided 2017-01-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005213332 SCV005852749 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-06-15 criteria provided, single submitter clinical testing

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