ClinVar Miner

Submissions for variant NM_000558.5(HBA1):c.273G>C (p.Lys91Asn) (rs33914470)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001000511 SCV001157416 likely benign none provided 2020-04-14 criteria provided, single submitter clinical testing
OMIM RCV000016999 SCV000037271 other HEMOGLOBIN BROUSSAIS 2018-05-10 no assertion criteria provided literature only
OMIM RCV000017000 SCV000037272 other HEMOGLOBIN J (BROUSSAIS) 2018-05-10 no assertion criteria provided literature only
OMIM RCV000017001 SCV000037273 other HEMOGLOBIN TAGAWA I 2018-05-10 no assertion criteria provided literature only

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