ClinVar Miner

Submissions for variant NM_001277269.1(OTOG):c.1376A>G (p.Asn459Ser) (rs115772736)

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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 RCV000614935 SCV000711518 benign not specified 2014-11-24 criteria provided, single submitter clinical testing Asn459Ser in exon 11 of OTOG: This variant is not expected to have clinical sign ificance because it has been identified in 3.1% (6/194) of Luhya (Kenyan) chromo somes from a broad population by the 1000 Genomes Project (http://www.ncbi.nlm.n ih.gov/projects/SNP; dbSNP rs115772736).
Invitae RCV000901952 SCV001046350 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000901952 SCV001768578 likely benign not provided 2021-02-19 criteria provided, single submitter clinical testing

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