ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.50641G>A (p.Gly16881Arg)

dbSNP: rs1559780843
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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 RCV001170831 SCV001333451 uncertain significance Cardiomyopathy 2017-11-29 criteria provided, single submitter clinical testing

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