ClinVar Miner

List of variants in gene AGL reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 111
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HGVS dbSNP gnomAD frequency
NM_000642.3(AGL):c.4481+245G>C rs114982938 0.03092
NM_000642.3(AGL):c.3363-51A>G rs572231 0.01985
NM_000642.3(AGL):c.3588+36T>G rs548255 0.01966
NM_000642.3(AGL):c.3363-344T>C rs17121583 0.01892
NM_000642.3(AGL):c.4481+307A>G rs138023651 0.01788
NM_000642.3(AGL):c.294-122T>C rs3766593 0.01684
NM_000642.3(AGL):c.4482-274A>G rs141576159 0.01645
NM_000642.3(AGL):c.664+52C>T rs149552795 0.01525
NM_000642.3(AGL):c.83-93C>G rs41285736 0.01525
NM_000642.3(AGL):c.460+81T>G rs114575037 0.01524
NM_000642.3(AGL):c.83-386A>G rs146291089 0.01523
NM_000642.3(AGL):c.82+1565T>G rs145049634 0.01521
NM_000642.3(AGL):c.3083+307T>A rs79691966 0.01460
NM_000642.3(AGL):c.2813-289C>G rs76784737 0.01457
NM_000642.3(AGL):c.2681+58C>T rs28730703 0.01361
NM_000642.3(AGL):c.1082+88G>A rs142990156 0.01325
NM_000642.3(AGL):c.3363-343G>A rs12734255 0.01279
NM_000642.3(AGL):c.1612-24C>A rs115666491 0.01263
NM_000642.3(AGL):c.4162-89T>A rs28730707 0.01226
NM_000642.3(AGL):c.3701-211T>C rs11166374 0.01219
NM_000642.3(AGL):c.3700+236G>A rs112278239 0.01147
NM_000642.3(AGL):c.3701-65A>C rs72970917 0.01118
NM_000642.3(AGL):c.2308+172T>C rs76321904 0.00979
NM_000642.3(AGL):c.1082+76_1082+78del rs113437474 0.00923
NM_000642.3(AGL):c.3949+62G>A rs79794510 0.00815
NM_000642.3(AGL):c.1083-120G>C rs114767209 0.00807
NM_000642.3(AGL):c.4482-229T>C rs12141927 0.00772
NM_000642.3(AGL):c.2812+96A>G rs145604857 0.00756
NM_000642.3(AGL):c.1423+124G>T rs489681 0.00729
NM_000642.3(AGL):c.3083+52A>G rs590623 0.00727
NM_000642.3(AGL):c.2813-103A>C rs685108 0.00699
NM_000642.3(AGL):c.3260-264A>G rs151199832 0.00677
NM_000642.3(AGL):c.82+276T>C rs140914380 0.00623
NM_000642.3(AGL):c.82+1354T>A rs146547795 0.00607
NM_000642.3(AGL):c.3362+249T>C rs112267398 0.00484
NM_000642.3(AGL):c.2813-177T>C rs115023183 0.00461
NM_000642.3(AGL):c.2682-39A>T rs78318902 0.00459
NM_000642.3(AGL):c.2813-23A>G rs76758694 0.00459
NM_000642.3(AGL):c.4162-123T>A rs75708138 0.00417
NM_000642.3(AGL):c.1424-164T>A rs142107235 0.00404
NM_000642.3(AGL):c.2813-126G>A rs143427634 0.00404
NM_000642.3(AGL):c.3259+26A>G rs12073608 0.00399
NM_000642.3(AGL):c.3384G>A (p.Ala1128=) rs149393587 0.00383
NM_000642.3(AGL):c.3701-77G>A rs545103312 0.00379
NM_000642.3(AGL):c.2002-55A>T rs74855268 0.00377
NM_000642.3(AGL):c.3701-159G>A rs115302979 0.00377
NM_000642.3(AGL):c.2883A>G (p.Arg961=) rs113625417 0.00375
NM_000642.3(AGL):c.3362+22T>A rs79435569 0.00373
NM_000642.3(AGL):c.3950-238A>G rs79222466 0.00336
NM_000642.3(AGL):c.3083+84C>A rs377410347 0.00333
NM_000642.3(AGL):c.1284-325C>T rs139450793 0.00327
NM_000642.3(AGL):c.665-43A>G rs150182025 0.00327
NM_000642.3(AGL):c.83-353G>C rs148506168 0.00323
NM_000642.3(AGL):c.2390A>G (p.Asn797Ser) rs149210307 0.00212
NM_000642.3(AGL):c.2546+10T>C rs74551473 0.00212
NM_000642.3(AGL):c.3259+49G>A rs180688996 0.00198
NM_000642.3(AGL):c.3203A>G (p.Tyr1068Cys) rs147165298 0.00193
NM_000642.3(AGL):c.1885G>A (p.Glu629Lys) rs146041189 0.00160
NM_000642.3(AGL):c.3792A>T (p.Gly1264=) rs148606237 0.00151
NM_000642.3(AGL):c.1875G>T (p.Thr625=) rs141944878 0.00143
NM_000642.3(AGL):c.3588+29G>T rs201885902 0.00134
NM_000642.3(AGL):c.968G>A (p.Arg323Gln) rs139399527 0.00123
NM_000642.3(AGL):c.2949+20C>T rs201729914 0.00114
NM_000642.3(AGL):c.1908A>G (p.Ser636=) rs144723143 0.00051
NM_000642.3(AGL):c.3822C>T (p.Ile1274=) rs143885684 0.00049
NM_000642.3(AGL):c.39C>T (p.Asn13=) rs138203039 0.00045
NM_000642.3(AGL):c.3589-19C>T rs368244330 0.00034
NM_000642.3(AGL):c.83-34A>G rs200998407 0.00030
NM_000642.3(AGL):c.82+4A>C rs765098686 0.00029
NM_000642.3(AGL):c.3700+14A>G rs368141566 0.00016
NM_000642.3(AGL):c.4027G>A (p.Glu1343Lys) rs112795811 0.00014
NM_000642.3(AGL):c.846+14G>A rs376827010 0.00014
NM_000642.3(AGL):c.3231G>A (p.Lys1077=) rs138063386 0.00011
NM_000642.3(AGL):c.1284-4A>G rs372612377 0.00010
NM_000642.3(AGL):c.1602C>T (p.His534=) rs563472929 0.00009
NM_000642.3(AGL):c.3696C>T (p.Asp1232=) rs143076729 0.00009
NM_000642.3(AGL):c.-76C>G rs888498974 0.00007
NM_000642.3(AGL):c.4164C>G (p.Ala1388=) rs142809832 0.00007
NM_000642.3(AGL):c.103T>C (p.Leu35=) rs370307706 0.00006
NM_000642.3(AGL):c.293+3A>G rs375459662 0.00006
NM_000642.3(AGL):c.261A>G (p.Gln87=) rs370304606 0.00005
NM_000642.3(AGL):c.-69+11G>C rs1057523356 0.00003
NM_000642.3(AGL):c.2814T>G (p.Gly938=) rs147590282 0.00003
NM_000642.3(AGL):c.3345A>T (p.Gly1115=) rs758265909 0.00003
NM_000642.3(AGL):c.1900-6T>C rs749096703 0.00002
NM_000642.3(AGL):c.4539C>T (p.Phe1513=) rs752519483 0.00002
NM_000642.3(AGL):c.959-15T>C rs1159446395 0.00002
NM_000642.3(AGL):c.1062A>G (p.Leu354=) rs1165052196 0.00001
NM_000642.3(AGL):c.1082+4T>A rs781204563 0.00001
NM_000642.3(AGL):c.1612-10C>G rs1057524368 0.00001
NM_000642.3(AGL):c.2337T>C (p.Ala779=) rs928189171 0.00001
NM_000642.3(AGL):c.2571A>G (p.Gln857=) rs373619867 0.00001
NM_000642.3(AGL):c.366A>G (p.Leu122=) rs1386596170 0.00001
NM_000642.3(AGL):c.3741T>C (p.Phe1247=) rs1279212438 0.00001
NM_000642.3(AGL):c.1319C>T (p.Ser440Phe) rs149771710
NM_000642.3(AGL):c.1612-236TTC[2] rs367874912
NM_000642.3(AGL):c.2001+8_2001+9delinsCT rs1064794512
NM_000642.3(AGL):c.2158-18_2158-16del rs770934299
NM_000642.3(AGL):c.2308+16A>G rs1553186633
NM_000642.3(AGL):c.2434-19del rs1553187226
NM_000642.3(AGL):c.3701-5T>G rs1057523410
NM_000642.3(AGL):c.4119T>C (p.Cys1373=) rs1057521342
NM_000642.3(AGL):c.4259+135del rs368705786
NM_000642.3(AGL):c.4259+79_4259+80dup rs11438303
NM_000642.3(AGL):c.4482-18G>A rs1057521645
NM_000642.3(AGL):c.4482-19T>C rs370127763
NM_000642.3(AGL):c.847-20dup rs771807071
NM_000642.3(AGL):c.954A>G (p.Thr318=) rs1057523817
NM_000642.3(AGL):c.959-19_959-18insATCTTTTCTTTCTTTTA rs761998241
NM_000642.3(AGL):c.959-53A>T rs184400307
NM_000642.3(AGL):c.959-61_959-60insTGACAGTTATAATCTCTTTGTAGATATTTGCATTTAAGGTATCATCTTTTCTTTCTTTTAGAAAATAG rs1064794576

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