ClinVar Miner

Submissions for variant NM_000169.2(GLA):c.1000-22C>T (rs2071228)

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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 RCV000250822 SCV000330963 benign not specified 2015-07-22 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000675279 SCV000800935 benign not provided 2015-10-23 no assertion criteria provided clinical testing
PreventionGenetics RCV000250822 SCV000302833 benign not specified criteria provided, single submitter clinical testing

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