ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.420T>A (p.Asn140Lys)

dbSNP: rs34240441
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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 RCV003736539 SCV004565192 likely benign not provided 2023-11-22 criteria provided, single submitter clinical testing
OMIM RCV000016381 SCV000036649 other HEMOGLOBIN HINSDALE 2017-12-12 no assertion criteria provided literature only

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