ClinVar Miner

Submissions for variant NM_005033.3(EXOSC9):c.66+48C>G

gnomAD frequency: 0.31224  dbSNP: rs3811742
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 RCV001609774 SCV001839751 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001609774 SCV005302666 benign not provided criteria provided, single submitter not provided

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