ClinVar Miner

Submissions for variant NM_000559.3(HBG1):c.*5A>C

dbSNP: rs1065686
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002227281 SCV002047705 benign Hereditary persistence of fetal hemoglobin 2023-09-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718979 SCV005323395 benign not provided criteria provided, single submitter not provided

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