ClinVar Miner

Submissions for variant NM_000046.5(ARSB):c.972A>G (p.Gly324=) (rs72762973)

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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 RCV000078006 SCV000109844 benign not specified 2012-07-13 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000381815 SCV000458385 likely benign Mucopolysaccharidosis type VI 2016-06-14 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000675206 SCV000800848 benign not provided 2015-10-22 no assertion criteria provided clinical testing
PreventionGenetics RCV000078006 SCV000301621 benign not specified criteria provided, single submitter clinical testing

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