ClinVar Miner

Submissions for variant NM_000517.6(HBA2):c.237C>G (p.Asn79Lys)

dbSNP: rs281860607
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001002325 SCV001160219 benign not specified 2019-01-30 criteria provided, single submitter clinical testing

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