ClinVar Miner

Submissions for variant NM_001277269.1(OTOG):c.8227-12C>A (rs11828989)

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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, Partners HealthCare Personalized Medicine RCV000220207 SCV000269529 benign not specified 2014-11-24 criteria provided, single submitter clinical testing 8227-12C>A in intron 50 of OTOG: This variant is not expected to have clinical s ignificance because it has been identified in 5.1% (9/176) of Yoruba (Nigerian) chromosomes from a broad population by the 1000 Genomes Project (http://www.ncbi .nlm.nih.gov/projects/SNP; dbSNP rs11828989).
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000433817 SCV000510608 benign not provided 2016-07-22 criteria provided, single submitter clinical testing
GeneDx RCV000433817 SCV001894475 benign not provided 2019-08-23 criteria provided, single submitter clinical testing

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