ClinVar Miner

Submissions for variant NM_001166355.2(LFNG):c.163_166dup (p.Glu56delinsGlyTer)

dbSNP: rs34637446
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000722464 SCV001849241 benign not provided 2020-11-25 criteria provided, single submitter clinical testing
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001529407 SCV001984125 benign not specified 2020-06-25 criteria provided, single submitter clinical testing
Gharavi Laboratory, Columbia University RCV000722464 SCV000853595 uncertain significance not provided 2018-09-16 no assertion criteria provided research
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529407 SCV001742804 benign not specified no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000722464 SCV001798567 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000722464 SCV001971855 likely benign not provided no assertion criteria provided clinical testing

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