ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.89250C>T (p.Ser29750=)

dbSNP: rs1559221602
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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) RCV000733820 SCV000861920 uncertain significance not provided 2018-06-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001439304 SCV001642189 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-11-15 criteria provided, single submitter clinical testing

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