ClinVar Miner

Submissions for variant NM_018117.12(WDR11):c.86+28A>G

gnomAD frequency: 0.01132  dbSNP: rs78163411
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 RCV001588775 SCV001824516 likely benign not provided 2018-11-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001588775 SCV005220234 likely benign not provided criteria provided, single submitter not provided

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