ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.5409-16del

dbSNP: rs2102365749
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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 RCV002115829 SCV002409014 benign Charcot-Marie-Tooth disease type 2 2021-07-05 criteria provided, single submitter clinical testing

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