ClinVar Miner

List of variants in gene GABRG2 reported as benign

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Total variants: 41
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HGVS dbSNP
NM_198903.2(GABRG2):c.*2120_*2121del rs34705786
NM_198903.2(GABRG2):c.*609C>T rs418210
NM_198903.2(GABRG2):c.*661T>A rs424740
NM_198903.2(GABRG2):c.-154C>T rs3219203
NM_198903.2(GABRG2):c.-4dup rs771282908
NM_198903.2(GABRG2):c.1042+108A>C
NM_198903.2(GABRG2):c.1042+20G>A rs11575991
NM_198903.2(GABRG2):c.1042+6A>G rs375294947
NM_198903.2(GABRG2):c.107+12C>T rs369466385
NM_198903.2(GABRG2):c.1248+99C>A
NM_198903.2(GABRG2):c.1356C>T (p.Tyr452=) rs749951528
NM_198903.2(GABRG2):c.1374C>T (p.Asp458=) rs113085352
NM_198903.2(GABRG2):c.243T>A (p.Leu81=) rs143295869
NM_198903.2(GABRG2):c.259+20G>A rs200011382
NM_198903.2(GABRG2):c.315C>T (p.Asn105=) rs11135176
NM_198903.2(GABRG2):c.327+12A>C rs188717038
NM_198903.2(GABRG2):c.328-20T>G rs74810777
NM_198903.2(GABRG2):c.354G>A (p.Ala118=) rs61735412
NM_198903.2(GABRG2):c.360G>A (p.Thr120=) rs77298346
NM_198903.2(GABRG2):c.409T>C (p.Leu137=) rs200828542
NM_198903.2(GABRG2):c.548+306C>T
NM_198903.2(GABRG2):c.588C>T (p.Asn196=) rs211037
NM_198903.2(GABRG2):c.631+18T>A rs145582456
NM_198903.2(GABRG2):c.632-191C>T
NM_198903.2(GABRG2):c.632-28TTGTT[5] rs1247520830
NM_198903.2(GABRG2):c.643A>G (p.Ile215Val)
NM_198903.2(GABRG2):c.678G>A (p.Ser226=) rs143065876
NM_198903.2(GABRG2):c.679G>T (p.Ala227Ser) rs148215078
NM_198903.2(GABRG2):c.703G>T (p.Gly235Cys)
NM_198903.2(GABRG2):c.705C>A (p.Gly235=) rs114972096
NM_198903.2(GABRG2):c.751+129C>T
NM_198903.2(GABRG2):c.751+4C>T rs587780948
NM_198903.2(GABRG2):c.751+52G>A
NM_198903.2(GABRG2):c.837A>G (p.Gln279=) rs78261481
NM_198903.2(GABRG2):c.888C>T (p.Ser296=) rs201672465
NM_198903.2(GABRG2):c.889+18A>G rs2422105
NM_198903.2(GABRG2):c.889+20A>C rs182866753
NM_198903.2(GABRG2):c.890-230A>T
NM_198903.2(GABRG2):c.890-81A>G
NM_198903.2(GABRG2):c.918T>C (p.Phe306=) rs115126975
NM_198903.2(GABRG2):c.960T>C (p.Tyr320=) rs558779533

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