ClinVar Miner

List of variants in gene GABRG2 reported as likely benign

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Total variants: 62
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HGVS dbSNP
NM_198903.2(GABRG2):c.*1497C>T rs11956247
NM_198903.2(GABRG2):c.*1518A>G rs567153845
NM_198903.2(GABRG2):c.*1636T>C rs551794496
NM_198903.2(GABRG2):c.*1974G>A rs150875037
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.-154C>T rs3219203
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.107+11C>A
NM_198903.2(GABRG2):c.107+223T>G
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
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.1248+14T>C rs779125212
NM_198903.2(GABRG2):c.1273-8C>T rs771660227
NM_198903.2(GABRG2):c.1292G>A (p.Arg431His) rs528036202
NM_198903.2(GABRG2):c.1315A>G (p.Met439Val) rs753097258
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.1509G>A (p.Leu503=) rs765904792
NM_198903.2(GABRG2):c.150T>C (p.Ala50=) rs1264403667
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=)
NM_198903.2(GABRG2):c.259+19C>T rs758196181
NM_198903.2(GABRG2):c.259+60A>T
NM_198903.2(GABRG2):c.260-16_260-15del rs747283752
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.36A>T (p.Ser12=) rs762058667
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.420C>T (p.Asn140=)
NM_198903.2(GABRG2):c.525T>C (p.Asp175=) rs770485021
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
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.963C>A (p.Ile321=)
NM_198903.2(GABRG2):c.99C>T (p.Leu33=) rs368162707

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