ClinVar Miner

Submissions for variant NM_000558.3(HBA1):c.154G>C (p.Gly52Arg)

dbSNP: rs33960522
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001283977 SCV001469510 uncertain significance not provided 2020-04-16 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001283977 SCV002048571 likely benign not provided 2021-10-25 criteria provided, single submitter clinical testing
OMIM RCV000017147 SCV000037419 other HEMOGLOBIN RUSS 2016-07-20 no assertion criteria provided literature only

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