ClinVar Miner

Submissions for variant NM_001277269.1(OTOG):c.4274G>A (p.Arg1425Gln) (rs143848095)

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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 RCV000611546 SCV000711520 likely benign not specified 2014-11-24 criteria provided, single submitter clinical testing Arg1425Gln in exon 33 of OTOG: This variant is not expected to have clinical sig nificance because it has been identified in 1.0% (5/492) of African chromosomes from a broad population by the 1000 Genomes Project (http://www.ncbi.nlm.nih.gov /projects/SNP; dbSNP rs143848095).
Invitae RCV000885546 SCV001028998 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000885546 SCV001144842 likely benign not provided 2018-11-14 criteria provided, single submitter clinical testing

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