ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.238G>A (p.Glu80Lys)

gnomAD frequency: 0.00001  dbSNP: rs772441887
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001277806 SCV002803851 uncertain significance Primary hyperoxaluria type 3 2022-05-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277806 SCV001464779 uncertain significance Primary hyperoxaluria type 3 2020-04-11 no assertion criteria provided clinical testing

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