ClinVar Miner

Submissions for variant NM_000517.6(HBA2):c.95+27C>T

gnomAD frequency: 0.00531  dbSNP: rs558457816
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ClinVar version:
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 RCV000759060 SCV000603880 likely benign not provided 2020-01-31 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759060 SCV000888141 benign not provided 2022-04-21 criteria provided, single submitter clinical testing

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