ClinVar Miner

Submissions for variant NM_003673.4(TCAP):c.494A>T (p.Gln165Leu)

dbSNP: rs2057253901
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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 RCV001170357 SCV001332931 uncertain significance Cardiomyopathy 2018-01-06 criteria provided, single submitter clinical testing

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