ClinVar Miner

Submissions for variant NM_002485.5(NBN):c.321-89T>A

gnomAD frequency: 0.02213  dbSNP: rs1805843
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 RCV001609859 SCV001839857 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001609859 SCV005264903 benign not provided criteria provided, single submitter not provided

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