ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.68465A>G (p.Asn22822Ser)

dbSNP: rs2046841251
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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 RCV003487164 SCV004240079 likely benign Cardiomyopathy 2023-06-26 criteria provided, single submitter clinical testing

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