ClinVar Miner

Submissions for variant NM_003361.4(UMOD):c.172G>A (p.Gly58Ser)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289275 SCV002579922 uncertain significance Familial juvenile hyperuricemic nephropathy type 1 2022-06-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002289275 SCV005638559 uncertain significance Familial juvenile hyperuricemic nephropathy type 1 2024-06-18 criteria provided, single submitter clinical testing

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