ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.32702A>C (p.Glu10901Ala)

dbSNP: rs2154274616
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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 RCV001799178 SCV002042443 uncertain significance Cardiomyopathy 2021-01-30 criteria provided, single submitter clinical testing

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