ClinVar Miner

Submissions for variant NM_031217.4(KIF18A):c.2535C>T (p.Asp845=)

gnomAD frequency: 0.00527  dbSNP: rs35440657
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000948863 SCV001095089 benign not provided 2018-02-25 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000948863 SCV004129957 likely benign not provided 2022-10-01 criteria provided, single submitter clinical testing KIF18A: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000948863 SCV005323025 benign not provided criteria provided, single submitter not provided

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