ClinVar Miner

Submissions for variant NM_006612.6(KIF1C):c.2301G>A (p.Gly767=)

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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 RCV005110862 SCV005728954 likely benign Spastic ataxia 2 2024-09-16 criteria provided, single submitter clinical testing

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