ClinVar Miner

Submissions for variant NM_004522.3(KIF5C):c.819+139T>A

gnomAD frequency: 0.01260  dbSNP: rs143758774
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001560239 SCV001782607 likely benign not provided 2018-08-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001560239 SCV005255812 likely benign not provided criteria provided, single submitter not provided

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