ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.57G>A (p.Val19=)

dbSNP: rs1554918177
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 RCV000586045 SCV000697140 likely benign not specified 2019-08-28 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000985754 SCV001134235 uncertain significance not provided 2019-02-21 criteria provided, single submitter clinical testing

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