ClinVar Miner

Submissions for variant NM_000531.6(OTC):c.867+35T>G (rs62622415)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000247322 SCV000304707 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000281 SCV001156917 benign Ornithine carbamoyltransferase deficiency 2018-09-12 criteria provided, single submitter clinical testing

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