ClinVar Miner

Submissions for variant NM_000030.3(AGXT):c.667A>C (p.Ser223Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Biochemistry Laboratory, Health Services Laboratory RCV003468707 SCV004217815 likely pathogenic Primary hyperoxaluria, type I 2023-10-27 criteria provided, single submitter curation ACMG:PM2 PM3 PP3 PP4

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