ClinVar Miner

Submissions for variant NM_004281.4(BAG3):c.670dup (p.Ser224fs)

dbSNP: rs1135402750
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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 Goettingen RCV000496997 SCV000588198 likely pathogenic Dilated cardiomyopathy 1HH 2017-05-23 no assertion criteria provided clinical testing Dilated Cardiomyopathy

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