ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18723C>G (p.Ser6241Arg)

dbSNP: rs1015857991
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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 RCV001799160 SCV002042388 uncertain significance Cardiomyopathy 2020-11-18 criteria provided, single submitter clinical testing

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