ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.294G>A (p.Gln98=)

gnomAD frequency: 0.00001  dbSNP: rs777208958
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000980484 SCV001128438 likely benign not provided 2024-06-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001273645 SCV002796087 likely benign Primary hyperoxaluria type 3 2021-11-14 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273645 SCV001456949 uncertain significance Primary hyperoxaluria type 3 2020-03-10 no assertion criteria provided clinical testing

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