ClinVar Miner

Submissions for variant NM_000289.6(PFKM):c.160-44A>G

gnomAD frequency: 0.00771  dbSNP: rs116172105
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247748 SCV000303482 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001559762 SCV001782060 likely benign not provided 2018-10-02 criteria provided, single submitter clinical testing

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