ClinVar Miner

Submissions for variant NM_000162.5(GCK):c.-281G>C

gnomAD frequency: 0.00058  dbSNP: rs570705419
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817445 SCV002068286 likely benign not specified 2018-01-17 criteria provided, single submitter clinical testing

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