ClinVar Miner

Submissions for variant NM_003239.5(TGFB3):c.-536del

dbSNP: rs71451199
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000270390 SCV000388867 uncertain significance Arrhythmogenic right ventricular cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002487390 SCV002788715 uncertain significance Arrhythmogenic right ventricular dysplasia 1; Rienhoff syndrome 2021-07-30 criteria provided, single submitter clinical testing

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