ClinVar Miner

List of variants in gene GABRG2 reported as uncertain significance by Invitae

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Total variants: 37
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HGVS dbSNP
NC_000005.9:g.(?_161528241)_(161582545_?)dup
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.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.1120G>A (p.Ala374Thr) rs398123523
NM_198903.2(GABRG2):c.1127A>G (p.Asp376Gly) rs1060501890
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.1292G>A (p.Arg431His) rs528036202
NM_198903.2(GABRG2):c.1317G>T (p.Met439Ile)
NM_198903.2(GABRG2):c.1399T>C (p.Cys467Arg)
NM_198903.2(GABRG2):c.1418G>A (p.Arg473Gln)
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.1513A>T (p.Asn505Tyr)
NM_198903.2(GABRG2):c.1535dup (p.Tyr512Ter)
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.353C>T (p.Ala118Val)
NM_198903.2(GABRG2):c.365A>G (p.Tyr122Cys) rs1554097875
NM_198903.2(GABRG2):c.41A>G (p.Tyr14Cys)
NM_198903.2(GABRG2):c.455T>C (p.Phe152Ser)
NM_198903.2(GABRG2):c.530G>A (p.Arg177Gln) rs1445637165
NM_198903.2(GABRG2):c.579A>G (p.Gln193=)
NM_198903.2(GABRG2):c.583C>A (p.His195Asn) rs981863613
NM_198903.2(GABRG2):c.608C>G (p.Ser203Cys) rs1334273668
NM_198903.2(GABRG2):c.71C>A (p.Thr24Lys) rs1060501891
NM_198903.2(GABRG2):c.764G>C (p.Arg255Pro) rs1561645172
NM_198903.2(GABRG2):c.764G>T (p.Arg255Leu)
NM_198903.2(GABRG2):c.811G>A (p.Asp271Asn) rs773065895
NM_198903.2(GABRG2):c.958T>G (p.Tyr320Asp)

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