ClinVar Miner

Submissions for variant NM_003361.4(UMOD):c.464G>C (p.Cys155Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005013914 SCV005638533 likely pathogenic Familial juvenile hyperuricemic nephropathy type 1 2024-04-23 criteria provided, single submitter clinical testing

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