ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.-92C>G (rs397515291)

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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 RCV000029963 SCV000052618 uncertain beta Thalassemia 2011-08-18 criteria provided, single submitter curation Converted during submission to Uncertain significance.
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759806 SCV000889381 uncertain significance not provided 2019-06-05 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508112 SCV001158861 benign not specified 2019-04-11 criteria provided, single submitter clinical testing

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