ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.93855A>T (p.Arg31285Ser)

dbSNP: rs1697824824
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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 RCV001171242 SCV001333946 uncertain significance Cardiomyopathy 2018-04-12 criteria provided, single submitter clinical testing

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