ClinVar Miner

Submissions for variant NM_173543.3(DZIP1L):c.1288+118T>A

gnomAD frequency: 0.64717  dbSNP: rs384828
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 RCV001681694 SCV001900710 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001681694 SCV005302377 benign not provided criteria provided, single submitter not provided

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