ClinVar Miner

List of variants in gene PPP1R3A reported as benign for glucose metabolism disease

Included ClinVar conditions (125):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002711.4(PPP1R3A):c.1428T>A (p.Asn476Lys) rs2974944 0.99641
NM_002711.4(PPP1R3A):c.1351G>A (p.Val451Met) rs2974942 0.97316
NM_002711.4(PPP1R3A):c.2645T>A (p.Leu882His) rs2974938 0.97161
NM_002711.4(PPP1R3A):c.1880G>A (p.Arg627Lys) rs35067467 0.03347
NM_002711.4(PPP1R3A):c.2649G>T (p.Arg883Ser) rs1800000 0.02352
NM_002711.4(PPP1R3A):c.1183T>G (p.Ser395Ala) rs62001864 0.01000
NM_002711.4(PPP1R3A):c.1835G>A (p.Gly612Glu) rs76910192 0.00825
NM_002711.4(PPP1R3A):c.1714A>G (p.Ile572Val) rs35398707 0.00796
NM_002711.4(PPP1R3A):c.3259A>G (p.Ile1087Val) rs77456357 0.00795
NM_002711.4(PPP1R3A):c.3044A>G (p.Asn1015Ser) rs149701175 0.00793
NM_002711.4(PPP1R3A):c.133G>A (p.Gly45Ser) rs8192687 0.00595
NM_002711.4(PPP1R3A):c.1915G>T (p.Gly639Cys) rs61756423 0.00493

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.