ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.1152T>C (p.Arg384=)

dbSNP: rs2102225734
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001411958 SCV001614030 likely benign Charcot-Marie-Tooth disease type 2 2019-12-04 criteria provided, single submitter clinical testing

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