ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.701-11_701-8dup (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 Clinical Services Laboratory,Illumina RCV000336697 SCV000366321 likely benign Primary hyperoxaluria 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV001513579 SCV001721221 benign not provided 2020-10-19 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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