ClinVar Miner

List of variants in gene MAGI2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 103
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012301.4(MAGI2):c.1225+164T>C rs17150560 0.03271
NM_012301.4(MAGI2):c.3915G>A (p.Gln1305=) rs117054456 0.02550
NM_012301.4(MAGI2):c.965+77_965+78del rs10641091 0.02530
NM_012301.4(MAGI2):c.3203+270A>G rs117818431 0.02323
NM_012301.4(MAGI2):c.1226-24T>C rs78879925 0.01612
NM_012301.4(MAGI2):c.2269+215T>G rs11763083 0.01586
NM_012301.4(MAGI2):c.1104-32C>T rs79679898 0.01571
NM_012301.4(MAGI2):c.539-173T>C rs75435882 0.01523
NM_012301.4(MAGI2):c.-27G>A rs115112916 0.01237
NM_012301.4(MAGI2):c.*99G>A rs77802301 0.01152
NM_012301.4(MAGI2):c.418+294C>T rs146770727 0.01137
NM_012301.4(MAGI2):c.3567+237T>G rs114505574 0.01026
NM_012301.4(MAGI2):c.2379C>T (p.Leu793=) rs73703715 0.00966
NM_012301.4(MAGI2):c.*66G>C rs188597942 0.00763
NM_012301.4(MAGI2):c.2329T>C (p.Leu777=) rs76346657 0.00722
NM_012301.4(MAGI2):c.1225+197C>A rs113234399 0.00628
NM_012301.4(MAGI2):c.276C>G (p.Pro92=) rs146012909 0.00597
NM_012301.4(MAGI2):c.3031+233C>A rs114618820 0.00481
NM_012301.4(MAGI2):c.1104-91C>T rs144816605 0.00368
NM_012301.4(MAGI2):c.900A>G (p.Glu300=) rs111635934 0.00217
NM_012301.4(MAGI2):c.3911G>A (p.Gly1304Asp) rs145648453 0.00206
NM_012301.4(MAGI2):c.2213G>A (p.Arg738Gln) rs145722885 0.00153
NM_012301.4(MAGI2):c.219C>T (p.Pro73=) rs148240352 0.00143
NM_012301.4(MAGI2):c.2454C>T (p.Arg818=) rs148580718 0.00081
NM_012301.4(MAGI2):c.3706+5G>A rs188293910 0.00060
NM_012301.4(MAGI2):c.3706+12G>A rs183407324 0.00043
NM_012301.4(MAGI2):c.4353G>A (p.Ser1451=) rs576579796 0.00040
NM_012301.4(MAGI2):c.3765C>T (p.Gly1255=) rs187773786 0.00039
NM_012301.4(MAGI2):c.411G>A (p.Thr137=) rs149568072 0.00024
NM_012301.4(MAGI2):c.1737C>T (p.Asp579=) rs142555732 0.00009
NM_012301.4(MAGI2):c.539-4G>C rs372292060 0.00005
NM_012301.4(MAGI2):c.948C>T (p.Gly316=) rs75675313 0.00004
NM_012301.4(MAGI2):c.1713C>T (p.Ser571=) rs587780386 0.00003
NM_012301.4(MAGI2):c.2846-16G>A rs780495015 0.00003
NM_012301.4(MAGI2):c.1425T>C (p.Tyr475=) rs148086431 0.00001
NM_012301.4(MAGI2):c.2270-16C>T rs1827620636 0.00001
NM_012301.4(MAGI2):c.2304T>C (p.Asp768=) rs779355676 0.00001
NM_012301.4(MAGI2):c.3114C>A (p.Pro1038=) rs1282358138 0.00001
NM_012301.4(MAGI2):c.3918G>A (p.Lys1306=) rs1325477273 0.00001
NM_012301.4(MAGI2):c.888A>G (p.Glu296=) rs761458674 0.00001
NC_000007.14:g.79453745G>T rs74394893
NC_000007.14:g.79453800GT[13] rs112104600
NM_012301.4(MAGI2):c.1158G>A (p.Lys386=)
NM_012301.4(MAGI2):c.1308T>C (p.Phe436=)
NM_012301.4(MAGI2):c.1332C>T (p.Asp444=)
NM_012301.4(MAGI2):c.1365G>C (p.Val455=)
NM_012301.4(MAGI2):c.1371G>A (p.Pro457=)
NM_012301.4(MAGI2):c.1409-6T>C
NM_012301.4(MAGI2):c.1515G>A (p.Val505=)
NM_012301.4(MAGI2):c.165G>A (p.Glu55=)
NM_012301.4(MAGI2):c.1743G>A (p.Thr581=)
NM_012301.4(MAGI2):c.1752G>A (p.Pro584=)
NM_012301.4(MAGI2):c.1845C>T (p.Phe615=)
NM_012301.4(MAGI2):c.1914T>G (p.Pro638=)
NM_012301.4(MAGI2):c.1929C>A (p.Gly643=)
NM_012301.4(MAGI2):c.2047+129_2047+132del rs374176014
NM_012301.4(MAGI2):c.2047+17C>T
NM_012301.4(MAGI2):c.2079+8G>A
NM_012301.4(MAGI2):c.2238C>T (p.Tyr746=)
NM_012301.4(MAGI2):c.2270-18C>T
NM_012301.4(MAGI2):c.2311+18C>G
NM_012301.4(MAGI2):c.2312-20T>C
NM_012301.4(MAGI2):c.2403+140del rs113984102
NM_012301.4(MAGI2):c.2433C>T (p.Gly811=)
NM_012301.4(MAGI2):c.2480A>T (p.Tyr827Phe)
NM_012301.4(MAGI2):c.2502C>T (p.Ala834=)
NM_012301.4(MAGI2):c.2520T>C (p.Tyr840=)
NM_012301.4(MAGI2):c.2541C>T (p.His847=)
NM_012301.4(MAGI2):c.2694C>T (p.His898=)
NM_012301.4(MAGI2):c.3039C>T (p.Asn1013=)
NM_012301.4(MAGI2):c.3051G>A (p.Ser1017=)
NM_012301.4(MAGI2):c.3204-18C>T
NM_012301.4(MAGI2):c.3204-67C>G
NM_012301.4(MAGI2):c.3285G>A (p.Pro1095=) rs1441158775
NM_012301.4(MAGI2):c.3424-14C>T
NM_012301.4(MAGI2):c.3424-19T>C
NM_012301.4(MAGI2):c.3567+14C>A
NM_012301.4(MAGI2):c.363G>T (p.Val121=)
NM_012301.4(MAGI2):c.3687G>A (p.Thr1229=)
NM_012301.4(MAGI2):c.3706+125TA[4] rs34931672
NM_012301.4(MAGI2):c.3706+12G>T
NM_012301.4(MAGI2):c.3707-143_3707-138dup rs1486229258
NM_012301.4(MAGI2):c.3707-17G>A
NM_012301.4(MAGI2):c.3707-9C>T
NM_012301.4(MAGI2):c.3855T>G (p.Thr1285=)
NM_012301.4(MAGI2):c.3879C>T (p.Asp1293=)
NM_012301.4(MAGI2):c.3951G>A (p.Ser1317=)
NM_012301.4(MAGI2):c.3981G>A (p.Arg1327=)
NM_012301.4(MAGI2):c.418+11T>C
NM_012301.4(MAGI2):c.418+11T>G
NM_012301.4(MAGI2):c.4216G>A (p.Ala1406Thr)
NM_012301.4(MAGI2):c.4221T>C (p.Gly1407=)
NM_012301.4(MAGI2):c.4305G>A (p.Lys1435=)
NM_012301.4(MAGI2):c.462T>C (p.Asp154=) rs1584893230
NM_012301.4(MAGI2):c.516C>T (p.Leu172=)
NM_012301.4(MAGI2):c.538+260CA[16] rs71085549
NM_012301.4(MAGI2):c.538+260CA[18] rs71085549
NM_012301.4(MAGI2):c.549C>T (p.Tyr183=)
NM_012301.4(MAGI2):c.564G>A (p.Pro188=)
NM_012301.4(MAGI2):c.588G>A (p.Leu196=)
NM_012301.4(MAGI2):c.648G>A (p.Lys216=)
NM_012301.4(MAGI2):c.965+266_965+270del rs201768226
NM_012301.4(MAGI2):c.966-7T>C rs984503694

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.