ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.2115+6944A>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005049915 SCV005678727 uncertain significance Charcot-Marie-Tooth disease type 2A1; Neuroblastoma, susceptibility to, 1 2024-03-26 criteria provided, single submitter clinical testing

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