ClinVar Miner

Submissions for variant NM_194248.3(OTOF):c.1580-6C>T (rs114260271)

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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 RCV000151608 SCV000199797 benign not specified 2012-04-30 criteria provided, single submitter clinical testing 1580-6C>T in Intron 14 of OTOF: This variant is not expected to have clinical si gnificance because it has been identified in 0.7% (25/3738) of African American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http: //evs.gs.washington.edu/EVS; dbSNP rs114260271).
Invitae RCV000971471 SCV001119123 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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