ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.39T>C (p.Thr13=)

dbSNP: rs1554918207
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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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 RCV000586539 SCV000697129 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing
Invitae RCV003574782 SCV004333495 likely benign not provided 2023-10-16 criteria provided, single submitter clinical testing

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