ClinVar Miner

Submissions for variant NM_000518.4(HBB):c.238G>A (p.Asp80Asn) (rs33990858)

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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 RCV000507382 SCV000603937 uncertain significance not specified 2016-12-13 criteria provided, single submitter clinical testing
OMIM RCV000016341 SCV000036609 other HEMOGLOBIN G (ACCRA) 2017-12-12 no assertion criteria provided literature only
OMIM RCV000030906 SCV000037078 other HEMOGLOBIN YAIZU 2017-12-12 no assertion criteria provided literature only

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