ClinVar Miner

List of variants in gene GABRG2 reported as uncertain significance

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Gene type:
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Total variants: 100
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HGVS dbSNP
GRCh37/hg19 5q34(chr5:161479977-161590162)x1
GRCh37/hg19 5q34(chr5:161555799-161624613)x1
NC_000005.9:g.(?_161528241)_(161582545_?)dup
NM_198903.2(GABRG2):c.*1320G>A rs886060385
NM_198903.2(GABRG2):c.*1392A>T rs886060386
NM_198903.2(GABRG2):c.*1427C>T rs375013278
NM_198903.2(GABRG2):c.*1468A>G rs372041761
NM_198903.2(GABRG2):c.*1763A>T rs886060387
NM_198903.2(GABRG2):c.*1889C>A rs886060388
NM_198903.2(GABRG2):c.*194G>A rs758832535
NM_198903.2(GABRG2):c.*1981G>C rs886060389
NM_198903.2(GABRG2):c.*247T>C rs371389067
NM_198903.2(GABRG2):c.*250A>C rs886060384
NM_198903.2(GABRG2):c.*32T>C rs749257839
NM_198903.2(GABRG2):c.*422C>T rs752382943
NM_198903.2(GABRG2):c.-104T>G rs886060380
NM_198903.2(GABRG2):c.-114T>C rs886060379
NM_198903.2(GABRG2):c.-179T>A rs886060378
NM_198903.2(GABRG2):c.-217C>G rs748771306
NM_198903.2(GABRG2):c.-241A>C rs886060377
NM_198903.2(GABRG2):c.-250C>T rs886060376
NM_198903.2(GABRG2):c.-268C>A rs886060375
NM_198903.2(GABRG2):c.-334C>T rs886060374
NM_198903.2(GABRG2):c.-4del rs771282908
NM_198903.2(GABRG2):c.-4dup rs771282908
NM_198903.2(GABRG2):c.1012A>G (p.Lys338Glu) rs1561658609
NM_198903.2(GABRG2):c.1016A>T (p.Asp339Val) rs1554100510
NM_198903.2(GABRG2):c.1027G>A (p.Ala343Thr)
NM_198903.2(GABRG2):c.1042+6A>G rs375294947
NM_198903.2(GABRG2):c.1047C>G (p.Ile349Met) rs1554100910
NM_198903.2(GABRG2):c.106G>A (p.Gly36Ser)
NM_198903.2(GABRG2):c.107+12C>T rs369466385
NM_198903.2(GABRG2):c.107+3A>G rs796052517
NM_198903.2(GABRG2):c.107+6A>G rs868452487
NM_198903.2(GABRG2):c.1072C>G (p.Leu358Val) rs1561660795
NM_198903.2(GABRG2):c.1087C>T (p.Arg363Trp) rs796052510
NM_198903.2(GABRG2):c.1094C>T (p.Ser365Leu)
NM_198903.2(GABRG2):c.1105G>T (p.Val369Phe) rs768061156
NM_198903.2(GABRG2):c.1120G>A (p.Ala374Thr) rs398123523
NM_198903.2(GABRG2):c.1127A>G (p.Asp376Gly) rs1060501890
NM_198903.2(GABRG2):c.1149C>G (p.Phe383Leu) rs796052511
NM_198903.2(GABRG2):c.11C>T (p.Pro4Leu) rs375295110
NM_198903.2(GABRG2):c.1207C>T (p.Arg403Trp) rs374512652
NM_198903.2(GABRG2):c.1208G>A (p.Arg403Gln) rs780199000
NM_198903.2(GABRG2):c.1230T>C (p.Asp410=) rs201824364
NM_198903.2(GABRG2):c.1232A>C (p.Lys411Thr) rs796052512
NM_198903.2(GABRG2):c.1233_1235del (p.Lys414del) rs727503941
NM_198903.2(GABRG2):c.1260G>A (p.Met420Ile) rs1554101092
NM_198903.2(GABRG2):c.1276C>T (p.Pro426Ser) rs757311213
NM_198903.2(GABRG2):c.1292G>A (p.Arg431His) rs528036202
NM_198903.2(GABRG2):c.1317G>T (p.Met439Ile)
NM_198903.2(GABRG2):c.135C>T (p.Asp45=) rs375308385
NM_198903.2(GABRG2):c.1399T>C (p.Cys467Arg)
NM_198903.2(GABRG2):c.13A>T (p.Asn5Tyr) rs774337016
NM_198903.2(GABRG2):c.1418G>A (p.Arg473Gln)
NM_198903.2(GABRG2):c.1433G>A (p.Arg478Lys) rs796052514
NM_198903.2(GABRG2):c.1440G>A (p.Gly480=) rs150727562
NM_198903.2(GABRG2):c.1454G>A (p.Arg485His) rs587780341
NM_198903.2(GABRG2):c.1454G>T (p.Arg485Leu) rs587780341
NM_198903.2(GABRG2):c.1480C>T (p.Arg494Trp) rs796052515
NM_198903.2(GABRG2):c.1509G>A (p.Leu503=) rs765904792
NM_198903.2(GABRG2):c.1513A>T (p.Asn505Tyr)
NM_198903.2(GABRG2):c.1535dup (p.Tyr512Ter)
NM_198903.2(GABRG2):c.1545G>A (p.Leu515=) rs886060383
NM_198903.2(GABRG2):c.173C>A (p.Thr58Asn)
NM_198903.2(GABRG2):c.17T>C (p.Ile6Thr)
NM_198903.2(GABRG2):c.191G>A (p.Gly64Asp) rs1408343754
NM_198903.2(GABRG2):c.21G>C (p.Trp7Cys) rs764172866
NM_198903.2(GABRG2):c.243T>A (p.Leu81=) rs143295869
NM_198903.2(GABRG2):c.247C>T (p.Pro83Ser) rs587777365
NM_198903.2(GABRG2):c.24C>A (p.Ser8Arg) rs183259247
NM_198903.2(GABRG2):c.269C>T (p.Thr90Met) rs1057520498
NM_198903.2(GABRG2):c.353C>T (p.Ala118Val)
NM_198903.2(GABRG2):c.365A>G (p.Tyr122Cys) rs1554097875
NM_198903.2(GABRG2):c.375T>A (p.Arg125=) rs767423340
NM_198903.2(GABRG2):c.41A>G (p.Tyr14Cys)
NM_198903.2(GABRG2):c.455T>C (p.Phe152Ser)
NM_198903.2(GABRG2):c.470A>C (p.Lys157Thr) rs770364855
NM_198903.2(GABRG2):c.530G>A (p.Arg177Gln) rs1445637165
NM_198903.2(GABRG2):c.549-3T>G rs750459631
NM_198903.2(GABRG2):c.571C>A (p.Gln191Lys) rs1334776746
NM_198903.2(GABRG2):c.579A>G (p.Gln193=)
NM_198903.2(GABRG2):c.582G>A (p.Leu194=) rs781498456
NM_198903.2(GABRG2):c.583C>A (p.His195Asn) rs981863613
NM_198903.2(GABRG2):c.596T>C (p.Met199Thr) rs770506471
NM_198903.2(GABRG2):c.608C>G (p.Ser203Cys) rs1334273668
NM_198903.2(GABRG2):c.649C>T (p.Gln217Ter) rs886645578
NM_198903.2(GABRG2):c.70A>G (p.Thr24Ala) rs796052516
NM_198903.2(GABRG2):c.71C>A (p.Thr24Lys) rs1060501891
NM_198903.2(GABRG2):c.751+4C>T rs587780948
NM_198903.2(GABRG2):c.764G>C (p.Arg255Pro) rs1561645172
NM_198903.2(GABRG2):c.764G>T (p.Arg255Leu)
NM_198903.2(GABRG2):c.810C>A (p.Gly270=) rs747988447
NM_198903.2(GABRG2):c.811G>A (p.Asp271Asn) rs773065895
NM_198903.2(GABRG2):c.868G>A (p.Glu290Lys) rs549251133
NM_198903.2(GABRG2):c.889+10A>G rs765703079
NM_198903.2(GABRG2):c.918T>C (p.Phe306=) rs115126975
NM_198903.2(GABRG2):c.928A>G (p.Arg310Gly) rs796052520
NM_198903.2(GABRG2):c.958T>G (p.Tyr320Asp)
NM_198903.2(GABRG2):c.973C>G (p.Leu325Val) rs1554100507

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