ClinVar Miner

Submissions for variant NM_017838.4(NHP2):c.*11T>A

gnomAD frequency: 0.00379  dbSNP: rs200781371
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251972 SCV000313035 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001575631 SCV001802672 likely benign not provided 2019-05-06 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000251972 SCV002069740 benign not specified 2019-01-03 criteria provided, single submitter clinical testing

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