ClinVar Miner

Submissions for variant NM_020242.3(KIF15):c.632C>T (p.Ala211Val)

gnomAD frequency: 0.00234  dbSNP: rs34862960
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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 RCV000890682 SCV001034447 likely benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000890682 SCV005260779 likely benign not provided criteria provided, single submitter not provided
CeGaT Center for Human Genetics Tuebingen RCV000890682 SCV005434355 likely benign not provided 2025-02-01 criteria provided, single submitter clinical testing KIF15: BS2

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