ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.7775T>G (p.Leu2592Arg)

dbSNP: rs2532652661
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Total submissions: 1
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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 RCV003487180 SCV004240128 likely benign Cardiomyopathy 2023-05-29 criteria provided, single submitter clinical testing

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