ClinVar Miner

Submissions for variant NM_006612.6(KIF1C):c.1666+13G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002828825 SCV003213872 benign Spastic ataxia 2 2024-05-15 criteria provided, single submitter clinical testing

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