ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.316-185C>T (rs1609812)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000243814 SCV000603885 benign not specified 2015-05-15 criteria provided, single submitter clinical testing
College of Science, Al Muthanna University,Al Muthanna University RCV000029983 SCV000864061 benign beta Thalassemia 2018-01-01 no assertion criteria provided research
Integrated Genetics/Laboratory Corporation of America RCV000029983 SCV000052638 benign beta Thalassemia 2011-08-18 criteria provided, single submitter curation Converted during submission to Benign.
PreventionGenetics RCV000243814 SCV000304632 benign not specified criteria provided, single submitter clinical testing

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