ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.3317G>A (p.Gly1106Asp)

dbSNP: rs2154349681
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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 RCV001799183 SCV002042449 uncertain significance Cardiomyopathy 2019-10-29 criteria provided, single submitter clinical testing

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