ClinVar Miner

List of variants in gene combination LOC121740717, PRKDC reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006904.7(PRKDC):c.8695C>T (p.Arg2899Cys) rs4278157 0.03559
NM_006904.7(PRKDC):c.8661C>T (p.Pro2887=) rs78163867 0.00528
NM_006904.7(PRKDC):c.8685G>A (p.Glu2895=) rs547408689

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.