ClinVar Miner

Submissions for variant NM_000558.5(HBA1):c.-42C>T (rs370305736)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507605 SCV000601194 likely benign not specified 2017-04-07 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001282579 SCV000603863 benign none provided 2020-03-17 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000755544 SCV000889343 likely benign not provided 2020-02-20 criteria provided, single submitter clinical testing
Natera, Inc. RCV001275683 SCV001461043 benign alpha Thalassemia 2020-09-16 no assertion criteria provided clinical testing

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