ClinVar Miner

Submissions for variant NM_003361.4(UMOD):c.840C>T (p.Pro280=)

dbSNP: rs78691203
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177174 SCV000229007 benign not specified 2014-05-27 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001824128 SCV000395536 benign Familial juvenile hyperuricemic nephropathy type 1 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics RCV001824128 SCV000677559 benign Familial juvenile hyperuricemic nephropathy type 1 2017-05-23 criteria provided, single submitter clinical testing
Invitae RCV000965325 SCV001112590 benign not provided 2024-01-23 criteria provided, single submitter clinical testing
GeneDx RCV000965325 SCV001898844 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002294064 SCV002587351 benign Kidney disorder 2018-05-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001824128 SCV002811293 likely benign Familial juvenile hyperuricemic nephropathy type 1 2021-09-14 criteria provided, single submitter clinical testing

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