ClinVar Miner

Submissions for variant NM_004281.4(BAG3):c.1257dup (p.Pro420fs)

dbSNP: rs2134069115
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001699749 SCV001922828 pathogenic not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001699749 SCV001958759 likely pathogenic not provided no assertion criteria provided clinical testing

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