ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.1191G>A (p.Pro397=) (rs25413)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000078001 SCV000109839 benign not specified 2014-10-13 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000372416 SCV000458379 benign Mucopolysaccharidosis type VI 2016-06-14 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000675201 SCV000800843 benign not provided 2017-04-12 no assertion criteria provided clinical testing
PreventionGenetics RCV000078001 SCV000301617 benign not specified criteria provided, single submitter clinical testing

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