ClinVar Miner

Submissions for variant NM_000517.6(HBA2):c.95+39C>G

gnomAD frequency: 0.00040  dbSNP: rs1025977498
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759061 SCV000888142 uncertain significance not provided 2017-12-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000759061 SCV001473497 likely benign not provided 2020-02-03 criteria provided, single submitter clinical testing

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