ClinVar Miner

Submissions for variant NM_001098511.3(KIF2A):c.1536G>A (p.Val512=)

gnomAD frequency: 0.00014  dbSNP: rs150906089
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720958 SCV001947319 benign not provided 2020-02-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001720958 SCV002396512 likely benign not provided 2023-12-09 criteria provided, single submitter clinical testing

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