ClinVar Miner

List of variants in gene CSNK2B reported by 3billion

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001320.7(CSNK2B):c.139C>T (p.Arg47Ter) rs1085307703
NM_001320.7(CSNK2B):c.292-2A>G rs1802000298
NM_001320.7(CSNK2B):c.332G>C (p.Arg111Pro) rs2151188333
NM_001320.7(CSNK2B):c.560T>G (p.Leu187Arg) rs1802055133
NM_001320.7(CSNK2B):c.569T>C (p.Phe190Ser) rs2536970927

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.