ClinVar Miner

List of variants in gene GABRG2 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 112
Download table as spreadsheet
HGVS dbSNP
NM_198903.2(GABRG2):c.*1518A>G rs567153845
NM_198903.2(GABRG2):c.*1636T>C rs551794496
NM_198903.2(GABRG2):c.*2095C>G rs138297122
NM_198903.2(GABRG2):c.*20A>C rs796052501
NM_198903.2(GABRG2):c.*261G>A rs148001179
NM_198903.2(GABRG2):c.*343A>G rs41275341
NM_198903.2(GABRG2):c.*385G>A rs185169107
NM_198903.2(GABRG2):c.*441T>C rs188825588
NM_198903.2(GABRG2):c.*794A>G rs73316347
NM_198903.2(GABRG2):c.*797G>T rs118064447
NM_198903.2(GABRG2):c.-4del rs771282908
NM_198903.2(GABRG2):c.1035A>G (p.Thr345=) rs1398214382
NM_198903.2(GABRG2):c.1042+6A>G rs375294947
NM_198903.2(GABRG2):c.1062A>G (p.Thr354=) rs377502016
NM_198903.2(GABRG2):c.1068C>A (p.Thr356=) rs1207623268
NM_198903.2(GABRG2):c.107+11C>A rs376576632
NM_198903.2(GABRG2):c.107+223T>G rs149245576
NM_198903.2(GABRG2):c.107+6A>G rs868452487
NM_198903.2(GABRG2):c.1074C>T (p.Leu358=) rs749531013
NM_198903.2(GABRG2):c.108-182G>A rs146492172
NM_198903.2(GABRG2):c.1095G>A (p.Ser365=) rs774809218
NM_198903.2(GABRG2):c.1122G>A (p.Ala374=) rs371601817
NM_198903.2(GABRG2):c.1134T>C (p.Phe378=) rs1057521488
NM_198903.2(GABRG2):c.11C>T (p.Pro4Leu) rs375295110
NM_198903.2(GABRG2):c.1242A>G (p.Lys414=) rs776166431
NM_198903.2(GABRG2):c.1248+14T>C rs779125212
NM_198903.2(GABRG2):c.1248+9C>T rs771223451
NM_198903.2(GABRG2):c.1273-7G>A rs372884176
NM_198903.2(GABRG2):c.1273-8C>G rs771660227
NM_198903.2(GABRG2):c.1273-8C>T rs771660227
NM_198903.2(GABRG2):c.1290C>A (p.Ile430=) rs1312081444
NM_198903.2(GABRG2):c.1302A>G (p.Ser434=) rs1458041410
NM_198903.2(GABRG2):c.1315A>G (p.Met439Val) rs753097258
NM_198903.2(GABRG2):c.1327A>G (p.Thr443Ala) rs757868774
NM_198903.2(GABRG2):c.1356C>T (p.Tyr452=) rs749951528
NM_198903.2(GABRG2):c.135C>T (p.Asp45=) rs375308385
NM_198903.2(GABRG2):c.1374C>T (p.Asp458=) rs113085352
NM_198903.2(GABRG2):c.1404T>C (p.Cys468=) rs141138508
NM_198903.2(GABRG2):c.1440G>A (p.Gly480=) rs150727562
NM_198903.2(GABRG2):c.1470C>T (p.Asp490=) rs202246006
NM_198903.2(GABRG2):c.1509G>A (p.Leu503=) rs765904792
NM_198903.2(GABRG2):c.150T>C (p.Ala50=) rs1264403667
NM_198903.2(GABRG2):c.1518G>T (p.Leu506=) rs1581463326
NM_198903.2(GABRG2):c.15T>C (p.Asn5=) rs1057522820
NM_198903.2(GABRG2):c.162A>G (p.Thr54=) rs748255945
NM_198903.2(GABRG2):c.219G>A (p.Leu73=) rs753076158
NM_198903.2(GABRG2):c.243T>A (p.Leu81=) rs143295869
NM_198903.2(GABRG2):c.259+19C>T rs758196181
NM_198903.2(GABRG2):c.259+60A>T rs78369083
NM_198903.2(GABRG2):c.260-16_260-15del rs747283752
NM_198903.2(GABRG2):c.260-9T>C rs1581345919
NM_198903.2(GABRG2):c.315C>T (p.Asn105=) rs11135176
NM_198903.2(GABRG2):c.333C>T (p.Tyr111=) rs777192588
NM_198903.2(GABRG2):c.354G>A (p.Ala118=) rs61735412
NM_198903.2(GABRG2):c.360G>A (p.Thr120=) rs77298346
NM_198903.2(GABRG2):c.36A>T (p.Ser12=) rs762058667
NM_198903.2(GABRG2):c.375T>A (p.Arg125=) rs767423340
NM_198903.2(GABRG2):c.37G>A (p.Val13Ile) rs796052502
NM_198903.2(GABRG2):c.402C>G (p.Val134=) rs562384157
NM_198903.2(GABRG2):c.41A>G (p.Tyr14Cys) rs61750979
NM_198903.2(GABRG2):c.420C>T (p.Asn140=) rs1581350860
NM_198903.2(GABRG2):c.525T>C (p.Asp175=) rs770485021
NM_198903.2(GABRG2):c.52G>C (p.Val18Leu) rs141106898
NM_198903.2(GABRG2):c.548+14A>G rs1057521821
NM_198903.2(GABRG2):c.574T>C (p.Leu192=) rs1554098050
NM_198903.2(GABRG2):c.588C>T (p.Asn196=) rs211037
NM_198903.2(GABRG2):c.752-8C>T rs779617978
NM_198903.2(GABRG2):c.810C>T (p.Gly270=) rs747988447
NM_198903.2(GABRG2):c.837A>G (p.Gln279=) rs78261481
NM_198903.2(GABRG2):c.84G>C (p.Leu28=) rs1554096092
NM_198903.2(GABRG2):c.888C>T (p.Ser296=) rs201672465
NM_198903.2(GABRG2):c.890-7G>A rs751069405
NM_198903.2(GABRG2):c.909T>G (p.Ser303=) rs754514348
NM_198903.2(GABRG2):c.90G>C (p.Leu30=) rs115976622
NM_198903.2(GABRG2):c.928A>C (p.Arg310=) rs796052520
NM_198903.2(GABRG2):c.963C>A (p.Ile321=) rs749127891
NM_198903.2(GABRG2):c.99C>T (p.Leu33=) rs368162707
NM_198903.2(GABRG2):c.9G>A (p.Ser3=) rs55716248
NM_198904.4(GABRG2):c.1158T>C (p.Pro386=)
NM_198904.4(GABRG2):c.1305A>G (p.Gly435=)
NM_198904.4(GABRG2):c.1356T>C (p.Tyr452=)
NM_198904.4(GABRG2):c.1362G>C (p.Arg454=)
NM_198904.4(GABRG2):c.1365C>A (p.Ile455=)
NM_198904.4(GABRG2):c.140A>G (p.Glu47Gly)
NM_198904.4(GABRG2):c.1413C>T (p.Ser471=)
NM_198904.4(GABRG2):c.143A>G (p.Asp48Gly) rs1581342183
NM_198904.4(GABRG2):c.184C>G (p.Pro62Ala)
NM_198904.4(GABRG2):c.185C>G (p.Pro62Arg)
NM_198904.4(GABRG2):c.243T>C (p.Leu81=)
NM_198904.4(GABRG2):c.260-8C>G
NM_198904.4(GABRG2):c.270G>A (p.Thr90=)
NM_198904.4(GABRG2):c.28G>A (p.Gly10Arg)
NM_198904.4(GABRG2):c.505A>T (p.Met169Leu)
NM_198904.4(GABRG2):c.552G>A (p.Leu184=)
NM_198904.4(GABRG2):c.567G>A (p.Glu189=)
NM_198904.4(GABRG2):c.573A>G (p.Gln191=)
NM_198904.4(GABRG2):c.632-1283C>G
NM_198904.4(GABRG2):c.632-6C>T
NM_198904.4(GABRG2):c.72G>C (p.Thr24=)
NM_198904.4(GABRG2):c.753A>C (p.Val251=)
NM_198904.4(GABRG2):c.759G>A (p.Lys253=)
NM_198904.4(GABRG2):c.75G>A (p.Val25=)
NM_198904.4(GABRG2):c.765T>G (p.Thr255=)
NM_198904.4(GABRG2):c.769+9C>A
NM_198904.4(GABRG2):c.79A>G (p.Ile27Val)
NM_198904.4(GABRG2):c.861C>T (p.Val287=)
NM_198904.4(GABRG2):c.93G>A (p.Leu31=)
NM_198904.4(GABRG2):c.972A>G (p.Lys324=)
NM_198904.4(GABRG2):c.981C>G (p.Pro327=)
NM_198904.4(GABRG2):c.987C>A (p.Val329=)
NM_198904.4(GABRG2):c.996C>T (p.Val332=)
NM_198904.4(GABRG2):c.999A>T (p.Thr333=)

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.