ClinVar Miner

List of variants in gene GABRG2 reported as likely benign by Invitae

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Total variants: 74
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HGVS dbSNP
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.1074C>T (p.Leu358=) rs749531013
NM_198903.2(GABRG2):c.1095G>A (p.Ser365=) rs774809218
NM_198903.2(GABRG2):c.1242A>G (p.Lys414=) rs776166431
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.1518G>T (p.Leu506=) rs1581463326
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.260-9T>C rs1581345919
NM_198903.2(GABRG2):c.333C>T (p.Tyr111=) rs777192588
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.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.52G>C (p.Val18Leu) rs141106898
NM_198903.2(GABRG2):c.752-8C>T rs779617978
NM_198903.2(GABRG2):c.810C>T (p.Gly270=) rs747988447
NM_198903.2(GABRG2):c.84G>C (p.Leu28=) rs1554096092
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.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.632-6C>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=)

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