ClinVar Miner

Submissions for variant NM_022114.4(PRDM16):c.1788C>G (p.Ser596Arg)

dbSNP: rs766972389
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV002052290 SCV002318938 uncertain significance Primary dilated cardiomyopathy no assertion criteria provided clinical testing

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