ClinVar Miner

Submissions for variant NM_006612.6(KIF1C):c.*61G>A

gnomAD frequency: 0.00258  dbSNP: rs146218874
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV001848491 SCV002105280 uncertain significance Hereditary spastic paraplegia 2016-12-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693778 SCV005192533 uncertain significance not provided criteria provided, single submitter not provided

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