ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.432C>T (p.His144=) (rs36020563)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000586720 SCV000697132 likely benign not specified 2020-09-17 criteria provided, single submitter clinical testing
Invitae RCV000861471 SCV001001796 benign not provided 2020-12-08 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001285480 SCV001471913 likely benign none provided 2020-06-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276401 SCV001462660 benign beta Thalassemia 2020-06-01 no assertion criteria provided clinical testing

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