ClinVar Miner

Submissions for variant NM_001039591.3(USP9X):c.655-56C>A

gnomAD frequency: 0.13515  dbSNP: rs41298468
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 RCV001649890 SCV001868247 benign not provided 2018-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001649890 SCV005276177 benign not provided criteria provided, single submitter not provided

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