ClinVar Miner

Submissions for variant NM_001715.3(BLK):c.1313-54C>A

gnomAD frequency: 0.42867  dbSNP: rs10097005
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 RCV001666065 SCV001882509 benign not provided 2018-08-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001666065 SCV005272387 benign not provided criteria provided, single submitter not provided

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