ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.9688A>G (p.Thr3230Ala)

dbSNP: rs1561180438
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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 RCV000769100 SCV000900473 uncertain significance Cardiomyopathy 2015-12-30 criteria provided, single submitter clinical testing

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