ClinVar Miner

List of variants in gene AGRN reported as benign by Preventiongenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.1178-6T>C rs2799066 0.86601
NM_198576.4(AGRN):c.2537-26A>G rs3128098 0.84465
NM_198576.4(AGRN):c.3558T>C (p.Phe1186=) rs10267 0.80748
NM_198576.4(AGRN):c.3066A>G (p.Ser1022=) rs2465128 0.79176
NM_198576.4(AGRN):c.3517-12T>C rs3128102 0.78058
NM_198576.4(AGRN):c.5651+5C>T rs9803031 0.77551
NM_198576.4(AGRN):c.1384+28G>A rs2710876 0.77416
NM_198576.4(AGRN):c.6057C>T (p.Asp2019=) rs4275402 0.58285
NM_198576.4(AGRN):c.4879+32G>A rs2799067 0.55443
NM_198576.4(AGRN):c.4161T>C (p.Thr1387=) rs9442391 0.49370
NM_198576.4(AGRN):c.4745-17C>T rs2275813 0.43854
NM_198576.4(AGRN):c.1385-15_1385-14del rs35881187 0.42851
NM_198576.4(AGRN):c.*19C>T rs3121561 0.35770
NM_198576.4(AGRN):c.4879+29G>T rs2275812 0.34370
NM_198576.4(AGRN):c.45G>T (p.Pro15=) rs115173026 0.30814
NM_198576.4(AGRN):c.5358T>C (p.Gly1786=) rs17160781 0.08292
NM_198576.4(AGRN):c.4514+16G>C rs112917612 0.06389
NM_198576.4(AGRN):c.3516+10G>C rs76264143 0.05034
NM_198576.4(AGRN):c.4996G>A (p.Val1666Ile) rs17160775 0.04750
NM_198576.4(AGRN):c.5070C>T (p.Phe1690=) rs17160776 0.04120
NM_198576.4(AGRN):c.2183A>T (p.Glu728Val) rs113288277 0.02946
NM_198576.4(AGRN):c.2555A>G (p.Gln852Arg) rs9697293 0.02583
NM_198576.4(AGRN):c.2254+16G>A rs114389542 0.02329
NM_198576.4(AGRN):c.4977-10A>G rs142286944 0.01828
NM_198576.4(AGRN):c.4740C>T (p.Arg1580=) rs115019873 0.01570
NM_198576.4(AGRN):c.3570C>T (p.Arg1190=) rs75361935 0.01197
NM_198576.4(AGRN):c.2025C>G (p.Gly675=) rs28484890 0.01118
NM_198576.4(AGRN):c.2406C>T (p.Gly802=) rs75774767 0.01095
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981 0.01049
NM_198576.4(AGRN):c.729C>G (p.Gly243=) rs191270495 0.00922
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser) rs138288952 0.00834
NM_198576.4(AGRN):c.738C>T (p.Asp246=) rs536085218 0.00811
NM_198576.4(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403 0.00799
NM_198576.4(AGRN):c.3972G>A (p.Pro1324=) rs201483077 0.00799
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381 0.00781
NM_198576.4(AGRN):c.1660G>A (p.Val554Met) rs79016973 0.00706
NM_198576.4(AGRN):c.1603+19G>A rs115191992 0.00697
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478 0.00691
NM_198576.4(AGRN):c.3077C>A (p.Thr1026Asn) rs3813188 0.00690
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=) rs146358566 0.00657
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803 0.00637
NM_198576.4(AGRN):c.5353G>A (p.Asp1785Asn) rs144245019 0.00636
NM_198576.4(AGRN):c.3404A>G (p.Gln1135Arg) rs142416636 0.00588
NM_198576.4(AGRN):c.5352C>T (p.Phe1784=) rs112073270 0.00537
NM_198576.4(AGRN):c.5025C>T (p.Gly1675=) rs147990356 0.00536
NM_198576.4(AGRN):c.1434G>A (p.Thr478=) rs147346337 0.00281
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541 0.00231
NM_198576.4(AGRN):c.5647G>A (p.Glu1883Lys) rs139415524 0.00167
NM_198576.4(AGRN):c.4298+11A>T rs369279324 0.00005
NM_198576.4(AGRN):c.2457G>C (p.Gly819=) rs112039851
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566

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.