ClinVar Miner

Submissions for variant NM_000558.5(HBA1):c.350A>C (p.Glu117Ala)

dbSNP: rs35932809
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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 RCV001811182 SCV001159465 likely benign not provided 2021-09-08 criteria provided, single submitter clinical testing
OMIM RCV000017177 SCV000037449 other HEMOGLOBIN UBE-4 2016-07-20 no assertion criteria provided literature only

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