ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.690-4571A>C

dbSNP: rs111941601
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000834674 SCV000976445 benign not provided 2018-06-19 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Breakthrough Genomics, Breakthrough Genomics RCV000834674 SCV005317604 benign not provided criteria provided, single submitter not provided
Cytogenetics- Mohapatra Lab, Banaras Hindu University RCV001293346 SCV001481934 uncertain significance Dilated cardiomyopathy 1C 2015-01-30 no assertion criteria provided case-control

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