ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.552G>T (p.Lys184Asn)

dbSNP: rs566113559
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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 RCV000768720 SCV000900090 uncertain significance Cardiomyopathy 2022-11-17 criteria provided, single submitter clinical testing

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