ClinVar Miner

Submissions for variant NM_006612.6(KIF1C):c.720+11C>T

dbSNP: rs770907929
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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 RCV002210238 SCV002369525 likely benign Spastic ataxia 2 2023-04-27 criteria provided, single submitter clinical testing

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