ClinVar Miner

Submissions for variant NM_000371.4(TTR):c.201-8C>A

dbSNP: rs1287386122
Minimum review status: Collection method:
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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 RCV003487207 SCV004240239 uncertain significance Cardiomyopathy 2023-05-04 criteria provided, single submitter clinical testing

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