ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.469-13C>T

dbSNP: rs750664684
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003669111 SCV004386523 likely benign not provided 2023-03-21 criteria provided, single submitter clinical testing
Clinical Biochemistry Laboratory, Health Services Laboratory RCV000186464 SCV000239822 uncertain significance Primary hyperoxaluria type 3 2014-11-27 no assertion criteria provided research

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