ClinVar Miner

List of variants in gene combination AGPS, LOC129935172 reported by PreventionGenetics, part of Exact Sciences

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_003659.4(AGPS):c.147C>T (p.Pro49=) rs34442536 0.01033
NM_003659.4(AGPS):c.192G>C (p.Ala64=) rs1218586614
NM_003659.4(AGPS):c.6G>A (p.Ala2=) rs755836525

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.