ClinVar Miner

Submissions for variant NM_000169.2(GLA):c.640-16A>G (rs2071397)

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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 RCV000078287 SCV000110127 benign not specified 2018-04-17 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000675280 SCV000800937 benign not provided 2015-12-15 no assertion criteria provided clinical testing
PreventionGenetics RCV000078287 SCV000302836 benign not specified criteria provided, single submitter clinical testing

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