ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.2115+6313G>T (rs374263753)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001002551 SCV001160522 uncertain significance not specified 2019-05-22 criteria provided, single submitter clinical testing

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