ClinVar Miner

Submissions for variant NC_000011.10:g.64590628G>A

gnomAD frequency: 0.03164  dbSNP: rs67048806
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 RCV001590553 SCV001825670 likely benign not provided 2020-05-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001590553 SCV005217416 likely benign not provided criteria provided, single submitter not provided

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