ClinVar Miner

Submissions for variant NM_000517.6(HBA2):c.22A>G (p.Lys8Glu)

dbSNP: rs34817956
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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 RCV003114197 SCV003799495 likely benign not provided 2022-04-02 criteria provided, single submitter clinical testing
OMIM RCV000016982 SCV000037254 other HEMOGLOBIN KUROSAKI 2016-10-13 no assertion criteria provided literature only

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