ClinVar Miner

List of variants in gene GABRB2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001371727.1(GABRB2):c.238-321G>A rs7713542 0.02295
NM_001371727.1(GABRB2):c.680-247C>T rs76403709 0.01998
NM_001371727.1(GABRB2):c.542-100A>G rs113714145 0.01627
NM_001371727.1(GABRB2):c.169+291A>G rs13178950 0.01564
NM_001371727.1(GABRB2):c.1191+254T>C rs138569742 0.01462
NM_001371727.1(GABRB2):c.542-191G>A rs72813518 0.01424
NM_001371727.1(GABRB2):c.680-174G>A rs112178828 0.01066
NM_001371727.1(GABRB2):c.458+125C>G rs55782657 0.01003
NM_001371727.1(GABRB2):c.541+273G>A rs77060612 0.00983
NM_001371727.1(GABRB2):c.170-176T>C rs116798629 0.00652
NM_001371727.1(GABRB2):c.1191+339C>T rs115619273 0.00467
NM_001371727.1(GABRB2):c.1191+264G>A rs73797569 0.00443
NM_001371727.1(GABRB2):c.680-118G>T rs73797577 0.00424
NM_001371727.1(GABRB2):c.832+241C>A rs73797576 0.00353
NM_001371727.1(GABRB2):c.832+236T>C rs147966597 0.00350
NM_001371727.1(GABRB2):c.542-233G>A rs148066109 0.00316
NM_001371727.1(GABRB2):c.237+21C>G rs192753738 0.00034
NM_001371727.1(GABRB2):c.-18C>G rs148024574 0.00026
NM_001371727.1(GABRB2):c.609G>A (p.Thr203=) rs138163747 0.00026
NM_001371727.1(GABRB2):c.77+18T>C rs200524787 0.00017
NM_001371727.1(GABRB2):c.1078-35G>A rs374012915 0.00014
NM_001371727.1(GABRB2):c.1159C>T (p.Arg387Trp) rs140795978 0.00014
NM_001371727.1(GABRB2):c.-19T>G rs373648067 0.00011
NM_001371727.1(GABRB2):c.1479A>T (p.Ile493=) rs750111998 0.00011
NM_021911.3(GABRB2):c.-136C>A rs890684223 0.00009
NM_001371727.1(GABRB2):c.1191G>A (p.Thr397=) rs373911261 0.00008
NM_001371727.1(GABRB2):c.237+12C>T rs371694224 0.00007
NM_001371727.1(GABRB2):c.594A>G (p.Ala198=) rs761307384 0.00007
NM_021911.3(GABRB2):c.-152-7A>T rs34758743 0.00007
NM_001371727.1(GABRB2):c.1103A>G (p.Asn368Ser) rs768489439 0.00006
NM_001371727.1(GABRB2):c.285G>A (p.Arg95=) rs144053366 0.00006
NM_001371727.1(GABRB2):c.1014A>G (p.Gln338=) rs747854210 0.00005
NM_001371727.1(GABRB2):c.1063C>T (p.Leu355=) rs764159075 0.00005
NM_001371727.1(GABRB2):c.1222A>C (p.Thr408Pro) rs200591388 0.00005
NM_001371727.1(GABRB2):c.1377T>C (p.His459=) rs201342925 0.00004
NM_001371727.1(GABRB2):c.1383G>A (p.Ala461=) rs536960677 0.00004
NM_001371727.1(GABRB2):c.357T>C (p.Asp119=) rs756503577 0.00004
NM_001371727.1(GABRB2):c.1118G>A (p.Arg373Gln) rs202183786 0.00003
NM_001371727.1(GABRB2):c.1153A>T (p.Thr385Ser) rs201397195 0.00003
NM_001371727.1(GABRB2):c.1410C>T (p.Arg470=) rs373821165 0.00003
NM_001371727.1(GABRB2):c.441C>T (p.Thr147=) rs370578958 0.00003
NM_021911.3(GABRB2):c.-153+3G>A rs892047281 0.00003
NM_021911.3(GABRB2):c.-156G>A rs1294667929 0.00003
NM_021911.3(GABRB2):c.-165A>G rs572328851 0.00003
NM_001371727.1(GABRB2):c.238-18T>C rs1485793918 0.00002
NM_001371727.1(GABRB2):c.459-15C>T rs759328020 0.00002
NM_001371727.1(GABRB2):c.60C>T (p.Ala20=) rs763231952 0.00002
NM_021911.3(GABRB2):c.-153+13T>G rs1054755645 0.00002
NM_001371727.1(GABRB2):c.-50T>C rs777888596 0.00001
NM_001371727.1(GABRB2):c.1077+6T>C rs993294374 0.00001
NM_001371727.1(GABRB2):c.1173C>T (p.Tyr391=) rs753777522 0.00001
NM_001371727.1(GABRB2):c.1320G>A (p.Gln440=) rs1184212049 0.00001
NM_001371727.1(GABRB2):c.141T>C (p.Tyr47=) rs909433122 0.00001
NM_001371727.1(GABRB2):c.679+7A>T rs1285127035 0.00001
NM_001371727.1(GABRB2):c.77+16G>T rs778830538 0.00001
NM_001371727.1(GABRB2):c.816T>A (p.Ala272=) rs766814600 0.00001
NM_001371727.1(GABRB2):c.9A>T (p.Arg3Ser) rs967225542 0.00001
NM_021911.3(GABRB2):c.-137C>T rs1193679437 0.00001
NM_001371727.1(GABRB2):c.*211C>T rs34906738
NM_001371727.1(GABRB2):c.169+8G>T rs1554107817
NM_001371727.1(GABRB2):c.170-11T>G rs1554107760
NM_001371727.1(GABRB2):c.171T>C (p.Gly57=) rs1554107757
NM_001371727.1(GABRB2):c.238-11C>T rs2113264228
NM_001371727.1(GABRB2):c.238-14del rs539366743
NM_001371727.1(GABRB2):c.238-14dup rs539366743
NM_001371727.1(GABRB2):c.542-58_542-57dup rs559725109
NM_001371727.1(GABRB2):c.578G>A (p.Arg193His) rs373324958
NM_001371727.1(GABRB2):c.723C>T (p.Asn241=) rs1057523200
NM_001371727.1(GABRB2):c.832+9T>C rs1057522438
NM_001371727.1(GABRB2):c.83A>G (p.Asn28Ser) rs1345193474
NM_021911.3(GABRB2):c.-153+9C>A rs1581076957

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