ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.896+6959C>T

gnomAD frequency: 0.00968  dbSNP: rs139415121
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000326083 SCV000365608 likely benign Myofibrillar myopathy 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000380800 SCV000365609 likely benign Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000291069 SCV000365610 likely benign Left ventricular noncompaction cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000346037 SCV000365611 likely benign Myofibrillar Myopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001582931 SCV001820581 likely benign not provided 2018-07-07 criteria provided, single submitter clinical testing

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