ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.174C>A (p.Asn58Lys) (rs35278874)

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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 RCV000506437 SCV000603936 uncertain significance not specified 2016-12-19 criteria provided, single submitter clinical testing
OMIM RCV000016347 SCV000036615 other HEMOGLOBIN G (FERRARA) 2017-12-12 no assertion criteria provided literature only

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