ClinVar Miner

Submissions for variant NM_138576.4(BCL11B):c.1742G>A (p.Gly581Asp)

dbSNP: rs775474405
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001349788 SCV001544148 benign not provided 2023-12-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001349788 SCV005194218 uncertain significance not provided criteria provided, single submitter not provided

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