ClinVar Miner

Submissions for variant NM_000558.3(HBA1):c.226G>T (p.Asp76Tyr)

dbSNP: rs33977363
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811183 SCV001472047 likely benign not provided 2021-03-09 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001811183 SCV002774603 uncertain significance not provided 2021-07-17 criteria provided, single submitter clinical testing
OMIM RCV000017179 SCV000037451 other HEMOGLOBIN WINNIPEG 2016-07-20 no assertion criteria provided literature only

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