ClinVar Miner

Submissions for variant NM_000184.2(HBG2):c.199A>C (p.Lys67Gln)

dbSNP: rs34264694
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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 RCV001811144 SCV002048155 likely benign not provided 2021-07-02 criteria provided, single submitter clinical testing
OMIM RCV000016127 SCV000036395 other HEMOGLOBIN F (BROOKLYN) 2011-08-05 no assertion criteria provided literature only

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