ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.316-184T>C (rs193922557)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000029982 SCV000052637 likely benign beta Thalassemia 2011-08-18 criteria provided, single submitter curation Converted during submission to Likely benign.
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508262 SCV000601280 likely benign not specified 2017-01-12 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759067 SCV000888149 likely benign not provided 2018-01-03 criteria provided, single submitter clinical testing

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