ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.33994+9A>C

dbSNP: rs2154268922
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799182 SCV002042448 uncertain significance Cardiomyopathy 2021-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077229 SCV002321524 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2021-02-22 criteria provided, single submitter clinical testing

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