ClinVar Miner

Submissions for variant NM_001626.6(AKT2):c.*9C>T

gnomAD frequency: 0.00890  dbSNP: rs79275829
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001818062 SCV002065952 benign not specified 2021-03-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704661 SCV005208350 likely benign not provided criteria provided, single submitter not provided

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