ClinVar Miner

Submissions for variant NM_018012.4(KIF26B):c.2605G>A (p.Gly869Arg)

gnomAD frequency: 0.00006  dbSNP: rs199690740
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
O&I group, Department of Genetics, University Medical Center of Groningen RCV001849205 SCV001960845 uncertain significance Autosomal dominant cerebellar ataxia 2021-07-22 no assertion criteria provided research

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