ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23496A>C (p.Arg7832Ser)

dbSNP: rs2154300468
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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 RCV001799166 SCV002042402 uncertain significance Cardiomyopathy 2019-08-26 criteria provided, single submitter clinical testing

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