ClinVar Miner

Submissions for variant NM_004523.4(KIF11):c.1806G>A (p.Gln602=)

gnomAD frequency: 0.01411  dbSNP: rs116840343
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000953303 SCV001099867 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV000953303 SCV001786334 likely benign not provided 2021-03-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000953303 SCV005221911 likely benign not provided criteria provided, single submitter not provided

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