ClinVar Miner

Submissions for variant NM_001128148.3(TFRC):c.1319-212T>A

dbSNP: rs499591
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
GeneDx RCV001611006 SCV001836675 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001611006 SCV005305734 benign not provided criteria provided, single submitter not provided

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