ClinVar Miner

List of variants in gene AGRN reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.3388+125T>C rs3128100 0.98469
NM_198576.4(AGRN):c.3388+176T>C rs3128101 0.90880
NM_198576.4(AGRN):c.2255-81G>A rs3128097 0.89344
NM_198576.4(AGRN):c.*156C>T rs2710872 0.87496
NM_198576.4(AGRN):c.2537-26A>G rs3128098 0.84465
NM_198576.4(AGRN):c.3388+107A>G rs3128099 0.80625
NM_198576.4(AGRN):c.1384+238C>T rs2710875 0.79091
NM_198576.4(AGRN):c.1384+28G>A rs2710876 0.77416
NM_198576.4(AGRN):c.5254-190C>T rs2710887 0.76955
NM_198576.4(AGRN):c.728-39C>A rs79290478 0.59863
NM_198576.4(AGRN):c.4879+32G>A rs2799067 0.55443
NM_198576.4(AGRN):c.4298+56del rs558237106 0.52555
NM_198576.4(AGRN):c.4879+33G>A rs397834473 0.48003
NM_198576.4(AGRN):c.4106-75_4106-74del rs140904842 0.45112
NM_198576.4(AGRN):c.1385-15_1385-14del rs35881187 0.42851
NM_198576.4(AGRN):c.1177+121G>C rs3121552 0.41548
NM_198576.4(AGRN):c.*56T>C rs2465136 0.39279
NM_198576.4(AGRN):c.4879+29G>T rs2275812 0.34370
NM_198576.4(AGRN):c.4879+43T>C rs2275811 0.20553
NM_198576.4(AGRN):c.*172G>A rs4308920 0.12261
NM_198576.4(AGRN):c.5876+143G>A rs72900467 0.08980
NM_198576.4(AGRN):c.4514+57A>G rs112331531 0.07657
NM_198576.4(AGRN):c.4106-214C>T rs113822357 0.06331
NM_198576.4(AGRN):c.4106-186C>T rs138543764 0.06122
NM_198576.4(AGRN):c.4106-145G>A rs149267690 0.05929
NM_198576.4(AGRN):c.4106-231G>A rs112285003 0.05827
NM_198576.4(AGRN):c.5253+69C>T rs55707163 0.05585
NM_198576.4(AGRN):c.5141+28G>T rs111726760 0.05398
NM_198576.4(AGRN):c.5253+68C>T rs112497350 0.05398
NM_198576.4(AGRN):c.5876+104G>A rs9778201 0.04896
NM_198576.4(AGRN):c.511+132G>A rs112116228 0.04843
NM_198576.4(AGRN):c.5141+39T>C rs116257587 0.04736
NM_198576.4(AGRN):c.804C>T (p.Ala268=) rs113789806 0.04656
NM_198576.4(AGRN):c.4745-44C>T rs115192323 0.04588
NM_198576.4(AGRN):c.3388+147C>T rs3813191 0.02471
NM_198576.4(AGRN):c.3388+145C>T rs3813190 0.02468
NM_198576.4(AGRN):c.2255-265C>T rs115449966 0.02321
NM_198576.4(AGRN):c.2254+258C>T rs116106396 0.02314
NM_198576.4(AGRN):c.2149-24G>A rs115413462 0.02269
NM_198576.4(AGRN):c.1058A>G (p.Gln353Arg) rs150359724 0.01713
NM_198576.4(AGRN):c.2254+71C>T rs116273657 0.01711
NM_198576.4(AGRN):c.512-264C>T rs116503955 0.01702
NM_198576.4(AGRN):c.4879+30G>T rs769247508 0.01575
NM_198576.4(AGRN):c.511+84G>A rs116010269 0.01523
NM_198576.4(AGRN):c.11G>C (p.Arg4Pro) rs539283387 0.01336
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.5223C>T (p.Gly1741=) rs147681220 0.00805
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381 0.00781
NM_198576.4(AGRN):c.4893C>T (p.Asp1631=) rs139400715 0.00732
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771 0.00700
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478 0.00691
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.1999+34C>T rs151102274 0.00589
NM_198576.4(AGRN):c.3404A>G (p.Gln1135Arg) rs142416636 0.00588
NM_198576.4(AGRN):c.5667G>A (p.Gln1889=) rs115061121 0.00532
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468 0.00517
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006 0.00426
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870 0.00302
NM_198576.4(AGRN):c.2067G>A (p.Gln689=) rs139886237 0.00288
NM_198576.4(AGRN):c.1434G>A (p.Thr478=) rs147346337 0.00281
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478 0.00225
NM_198576.4(AGRN):c.3765G>A (p.Ala1255=) rs149490453 0.00113
GRCh37/hg19 1p36.33(chr1:957640-964438)x0
GRCh37/hg19 1p36.33(chr1:963864-964438)x1
GRCh37/hg19 1p36.33(chr1:963864-986737)x0
GRCh37/hg19 1p36.33(chr1:963938-964438)x1
GRCh37/hg19 1p36.33(chr1:963938-985900)x1
NC_000001.11:g.1020068_1020069del rs569722974
NC_000001.11:g.1020069del rs569722974
NM_198576.4(AGRN):c.1177+109_1178-99del rs70949546
NM_198576.4(AGRN):c.2536+57del rs139005472
NM_198576.4(AGRN):c.3389-134C>T rs3813192
NM_198576.4(AGRN):c.4105+180C>A rs113521698
NM_198576.4(AGRN):c.4106-45A>G rs115499153
NM_198576.4(AGRN):c.4106-78dup rs57668569
NM_198576.4(AGRN):c.4106-81_4106-78del rs57668569
NM_198576.4(AGRN):c.4106-88_4106-78del rs57668569
NM_198576.4(AGRN):c.4298+55dup rs754994713
NM_198576.4(AGRN):c.4298+56_4298+57del rs567082250
NM_198576.4(AGRN):c.464-240A>C rs111329619
NM_198576.4(AGRN):c.4879+41del rs71576592
NM_198576.4(AGRN):c.511+211C>T rs115493882
NM_198576.4(AGRN):c.5141+67G>A rs28758798
NM_198576.4(AGRN):c.5141+67G>C rs28758798
NM_198576.4(AGRN):c.5652-201G>C rs2710871
NM_198576.4(AGRN):c.728-51_728-49del rs1266764583

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.