ClinVar Miner

Submissions for variant NM_001378743.1(CYLD):c.2242-46G>T

gnomAD frequency: 0.11696  dbSNP: rs10451132
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 RCV001714631 SCV001946342 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001714631 SCV005289798 benign not provided criteria provided, single submitter not provided

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