ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.896+6669TC[12]

dbSNP: rs71019410
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Mass General Brigham Personalized Medicine RCV000036851 SCV000060506 likely benign not specified 2011-10-12 criteria provided, single submitter clinical testing 756-15_756-12delCTCT in intron 7 of LDB3: This variant is not expected to have c linical significance because it is not located in the conserved +/- 1, 2 region of the splicing consensus sequence.
Eurofins NTD LLC (GA) RCV000036851 SCV000332565 benign not specified 2015-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001668154 SCV001883480 benign not provided 2019-08-13 criteria provided, single submitter clinical testing

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