ClinVar Miner

List of variants in gene GABRG2 reported as uncertain significance for not provided

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Total variants: 28
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HGVS dbSNP
GRCh37/hg19 5q34(chr5:161479977-161590162)x1
GRCh37/hg19 5q34(chr5:161555799-161624613)x1
NM_198903.2(GABRG2):c.1016A>T (p.Asp339Val) rs1554100510
NM_198903.2(GABRG2):c.107+3A>G rs796052517
NM_198903.2(GABRG2):c.1120G>A (p.Ala374Thr) rs398123523
NM_198903.2(GABRG2):c.1149C>G (p.Phe383Leu) rs796052511
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.1276C>T (p.Pro426Ser) rs757311213
NM_198903.2(GABRG2):c.13A>T (p.Asn5Tyr) rs774337016
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>T (p.Arg485Leu) rs587780341
NM_198903.2(GABRG2):c.247C>T (p.Pro83Ser) rs587777365
NM_198903.2(GABRG2):c.269C>T (p.Thr90Met) rs1057520498
NM_198903.2(GABRG2):c.470A>C (p.Lys157Thr) rs770364855
NM_198903.2(GABRG2):c.549-3T>G rs750459631
NM_198903.2(GABRG2):c.571C>A (p.Gln191Lys) rs1334776746
NM_198903.2(GABRG2):c.582G>A (p.Leu194=) rs781498456
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.811G>A (p.Asp271Asn) rs773065895
NM_198903.2(GABRG2):c.868G>A (p.Glu290Lys) rs549251133
NM_198903.2(GABRG2):c.918T>C (p.Phe306=) rs115126975
NM_198903.2(GABRG2):c.928A>G (p.Arg310Gly) rs796052520

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