ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.690-4619G>T

gnomAD frequency: 0.00006  dbSNP: rs761090088
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000364330 SCV000365580 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000276729 SCV000365581 uncertain significance Left ventricular noncompaction cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000334179 SCV000365582 uncertain significance Myofibrillar Myopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000386538 SCV000365583 uncertain significance Myofibrillar myopathy 4 2016-06-14 criteria provided, single submitter clinical testing

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