ClinVar Miner

Submissions for variant NM_020297.4(ABCC9):c.1165-4del

dbSNP: rs886049172
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000401977 SCV000377537 uncertain significance Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000287517 SCV000377538 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000342593 SCV000377539 uncertain significance Hypertrichotic osteochondrodysplasia Cantu type 2016-06-14 criteria provided, single submitter clinical testing

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