ClinVar Miner

Submissions for variant NM_016821.3(OGG1):c.1043G>A (p.Gly348Glu)

gnomAD frequency: 0.00054  dbSNP: rs41276495
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000625393 SCV000745225 likely benign Nonpapillary renal cell carcinoma 2017-05-10 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000625393 SCV000745855 likely benign Nonpapillary renal cell carcinoma 2016-01-22 no assertion criteria provided clinical testing

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