ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.700+67G>A (rs2297643)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Nilou-Genome Lab RCV000186467 SCV001754877 likely benign Primary hyperoxaluria, type III 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001698501 SCV001916785 benign not provided 2020-01-11 criteria provided, single submitter clinical testing
Clinical Biochemistry Laboratory,Health Services Laboratory RCV000186467 SCV000239825 uncertain significance Primary hyperoxaluria, type III 2014-11-27 no assertion criteria provided research

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