ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.315+26T>G

gnomAD frequency: 0.00234  dbSNP: rs368604295
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000860814 SCV000603891 benign not provided 2019-10-04 criteria provided, single submitter clinical testing
Invitae RCV000860814 SCV001000973 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Natera, Inc. RCV001272123 SCV001453775 benign beta Thalassemia 2020-09-16 no assertion criteria provided clinical testing

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