ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.*56A>T (rs537944366)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000337326 SCV000372524 uncertain significance Hb SS disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000405739 SCV000372525 uncertain significance Fetal hemoglobin quantitative trait locus 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000297689 SCV000372526 uncertain significance beta Thalassemia 2016-06-14 criteria provided, single submitter clinical testing

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