ClinVar Miner

Submissions for variant NM_001277269.1(OTOG):c.6329-7C>T (rs143985593)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000217116 SCV000269517 benign not specified 2014-11-24 criteria provided, single submitter clinical testing 6329-7C>T in intron 36 of OTOG: This variant is not expected to have clinical si gnificance because it has been identified in 6.8% (12/176) of Yoruba (Nigerian) chromosomes from a broad population by the 1000 Genomes Project (http://www.ncbi .nlm.nih.gov/projects/SNP; dbSNP rs143985593).
Invitae RCV000970221 SCV001117790 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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