ClinVar Miner

List of variants in gene AGL reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_000642.3(AGL):c.664+150T>C rs539157 0.76296
NM_000642.3(AGL):c.894C>T (p.Leu298=) rs2230306 0.76251
NM_000642.3(AGL):c.82+85C>T rs663848 0.76243
NM_000642.3(AGL):c.460+293G>A rs687979 0.76236
NM_000642.3(AGL):c.664+92A>G rs538389 0.75534
NM_000642.3(AGL):c.959-18G>A rs634880 0.73702
NM_000642.3(AGL):c.461-53G>C rs535461 0.72299
NM_000642.3(AGL):c.3259+288G>A rs515957 0.67524
NM_000642.3(AGL):c.3259+37G>A rs594249 0.65860
NM_000642.3(AGL):c.2812+11G>A rs555929 0.65828
NM_000642.3(AGL):c.2681+124G>A rs2234707 0.51021
NM_000642.3(AGL):c.1423+74C>T rs3736295 0.51012
NM_000642.3(AGL):c.2001+8T>C rs3736296 0.51012
NM_000642.3(AGL):c.2950-121A>G rs2035960 0.50971
NM_000642.3(AGL):c.3259+224_3259+228dup rs10628111 0.50840
NM_000642.3(AGL):c.1424-124T>A rs2291637 0.48276
NM_000642.3(AGL):c.2950-21T>A rs2035961 0.48240
NM_000642.3(AGL):c.3836+45G>A rs2274570 0.46505
NM_000642.3(AGL):c.3836+53T>A rs1541041 0.46492
NM_000642.3(AGL):c.-10A>G rs2307130 0.41188
NM_000642.3(AGL):c.3700+290A>G rs17121609 0.39978
NM_000642.3(AGL):c.4260-97G>A rs2296885 0.38982
NM_000642.3(AGL):c.3949+294A>T rs6692695 0.38955
NM_000642.3(AGL):c.665-73A>G rs903126 0.37617
NM_000642.3(AGL):c.4259+262T>C rs7555316 0.37598
NM_000642.3(AGL):c.2309-295A>C rs17409324 0.36899
NM_000642.3(AGL):c.*272G>T rs1804808 0.31955
NM_000642.3(AGL):c.293+212C>A rs3766592 0.31940
NM_000642.3(AGL):c.1424-44A>G rs2291638 0.29229
NM_000642.3(AGL):c.83-33C>T rs2307129 0.24077
NM_000642.3(AGL):c.665-168A>G rs67875069 0.24069
NM_000642.3(AGL):c.3837-172C>T rs3818568 0.13741
NM_000642.3(AGL):c.3199C>T (p.Pro1067Ser) rs3753494 0.13698
NM_000642.3(AGL):c.3362+236G>A rs4908034 0.13674
NM_000642.3(AGL):c.2308+216C>A rs1389381 0.13651
NM_000642.3(AGL):c.461-279A>C rs61434101 0.11285
NM_000642.3(AGL):c.3589-348G>A rs659030 0.06609
NM_000642.3(AGL):c.1736-213C>T rs12035706 0.05861
NM_000642.3(AGL):c.3343G>A (p.Gly1115Arg) rs2230307 0.05399
NM_000642.3(AGL):c.3700+32T>C rs834575 0.05338
NM_000642.3(AGL):c.3837-217T>C rs17121622 0.05331
NM_000642.3(AGL):c.461-271A>G rs11166361 0.04404
NM_000642.3(AGL):c.686A>G (p.Gln229Arg) rs17121403 0.04398
NM_000642.3(AGL):c.461-117G>T rs534662 0.03294
NM_000642.3(AGL):c.958+200C>T rs79253638 0.02949
NM_000642.3(AGL):c.2813-110C>T rs12086095 0.02346
NM_000642.3(AGL):c.1083-162A>G rs77858980 0.01951
NM_000642.3(AGL):c.1185+15T>C rs17121466 0.01894
NM_000642.3(AGL):c.1155G>T (p.Lys385Asn) rs28730701 0.01764
NM_000642.3(AGL):c.959-170A>G rs79132413 0.01681
NM_000642.3(AGL):c.207T>C (p.Asn69=) rs2230305 0.01529
NM_000642.3(AGL):c.112A>G (p.Thr38Ala) rs35278779 0.01527
NM_000642.3(AGL):c.2885C>G (p.Ser962Cys) rs34714252 0.01465
NM_000642.3(AGL):c.1160G>A (p.Arg387Gln) rs17121464 0.01447
NM_000642.3(AGL):c.3849T>C (p.Ala1283=) rs28730706 0.01312
NM_000642.3(AGL):c.3260-19G>A rs140333425 0.01279
NM_000642.3(AGL):c.3619G>A (p.Ala1207Thr) rs11807956 0.00940
NM_000642.3(AGL):c.2802A>C (p.Ala934=) rs34230588 0.00775
NM_000642.3(AGL):c.1481G>A (p.Arg494His) rs141043166 0.00743
NM_000642.3(AGL):c.4430C>G (p.Thr1477Ser) rs78348923 0.00530
NM_000642.3(AGL):c.3758G>A (p.Arg1253His) rs12043139 0.00515
NM_000642.3(AGL):c.3260-20T>C rs17121560 0.00332
NM_000642.3(AGL):c.2522C>T (p.Ser841Phe) rs150441555 0.00209
NM_000642.3(AGL):c.1612-338AATA[7] rs199927371
NM_000642.3(AGL):c.1612-70C>G rs2392077
NM_000642.3(AGL):c.3588+43_3588+44del rs35956186
NM_000642.3(AGL):c.3588+44dup rs35956186
NM_000642.3(AGL):c.4162-11G>A rs184309460
NM_000642.3(AGL):c.4259+80dup rs11438303
NM_000642.3(AGL):c.4260-151G>T rs6665958
NM_000642.3(AGL):c.665-196del rs530402620
NM_000642.3(AGL):c.82+1247_82+1248del rs11363065
NM_000642.3(AGL):c.82+1248del rs11363065
NM_000642.3(AGL):c.82+1432dup rs58176899
NM_000642.3(AGL):c.959-300T>C rs58794035

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