ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.91AAG[1] (p.Lys32del)

dbSNP: rs750736378
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665183 SCV000789256 uncertain significance Primary hyperoxaluria type 3 2017-01-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000665183 SCV002785539 uncertain significance Primary hyperoxaluria type 3 2022-05-26 criteria provided, single submitter clinical testing

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