ClinVar Miner

Submissions for variant NM_003361.3(UMOD):c.1372G>T (p.Val458Leu) (rs55772253)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000395450 SCV000345660 benign not specified 2016-09-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000359715 SCV000395528 benign Uromodulin-associated kidney disease 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576835 SCV000677558 benign Familial juvenile gout; Autosomal dominant medullary cystic kidney disease with hyperuricemia 2017-05-23 criteria provided, single submitter clinical testing

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