ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.701-11_701-8dup

dbSNP: rs143018385
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000336697 SCV000366321 likely benign Primary hyperoxaluria 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001513579 SCV001721221 benign not provided 2025-01-23 criteria provided, single submitter clinical testing
GeneDx RCV001513579 SCV001842566 benign not provided 2021-02-09 criteria provided, single submitter clinical testing

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